Torx 2030-6525-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 27 adverse event reports that list this exact device (DI 07613327036992), received between Jan 11, 2017 and Mar 9, 2023 — classified as 12 injuries, 15 malfunctions.

The most frequently reported specific device problem is “Break” (6 reports).

32 other recalls cover devices cleared under the same FDA submission (K873251, K894124); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 27 reports, in the reporter's own words as published by the FDA.

• InjuryMar 9, 2023Fracture; Fracture

  A PATIENT WHO UNDERWENT THA ON (B)(6) 2016, COMPLAINED OF RIGHT HIP PAIN. X-RAYS REVEALED THAT THE CUP SIDE WAS PROLAPSED. ONE SCREW (OUT OF THREE) WAS FOUND TO BE BROKEN WHEN THE CUP WAS REMOVED. THE MOLAR FLOOR WAS IN METALLOSIS. THE DOCTOR DECIDED TO LEAVE THE BROKEN SCREW IN PLACE AND PROCEEDED WITH THE OPERATION BECAUSE REMOVING THE ENTIRE SCREW WOULD BE TOO RISKY. AFTER THAT, THE OPERATION WAS COMPLETED AS PLANNED.

  Patient problems: Joint Dislocation; Metal Related Pathology; Pain

  MAUDE report 16513283 ↗
• MalfunctionDec 21, 2020Break; Break

  AS REPORTED: "SURGEON REVISING FAILED (RIGHT) HIP REPLACEMENT. IMPLANT LOG FROM PRIMARY SURGERY ATTACHED." UPDATE 12/04/2020 WG: SPOKE TO REP. PATIENT WAS REVISED DUE TO SUSPECTED CUP LOOSENING. INTRAOPERATIVELY THE CUP WAS FOUND LOOSE AND A SCREW WAS BROKEN. THE CUP AND SCREW WERE REMOVED. THE HEAD AND LINER WERE REMOVED BUT THERE ARE NO ALLEGATIONS AGAINST THEM. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Inadequate Osseointegration

  MAUDE report 11044537 ↗
• MalfunctionAug 20, 2020Fracture; Fracture

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO ASEPTIC LOOSENING OF THE SHELL AND TWO BROKEN SCREWS. INTRA-OPERATIVELY, WEAR WAS NOTED ON THE FEMORAL HEAD. THERE ARE NO ALLEGATIONS AGAINST THE REVISED LINER. PATIENT WAS REVISED TO A TRIDENT 2 SHELL, MDM METAL LINER, ADM/MDM POLY INSERT, AND A BIOLOX HEAD WITH SLEEVE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10435186 ↗
• InjuryAug 4, 2020Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO INSTABILITY AND DISLOCATION OF THE HEAD FROM THE POLY LINER. THE SHELL WAS REVISED DUE TO THE SURGEON NEEDING MORE ANTEVERSION. PATIENT WAS REVISED TO A 28MM + 12 MM L FIT V40 FEMORAL HEAD, A 28/52 MM RESTORATION ADM/MDM X3 INSERT, A 46 MM MDM CEMENTLESS LINER, AND 56 MM TRIDENT II CLUSTERHOLE HA SHELL WITH THREE 6.5MM X 15 MM SCREWS AND ONW 6.5 MM X 20 MM SCREW. REP CONFIRMED THAT NO FURTHER INFORMATION WOULD BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Injury

  MAUDE report 10364860 ↗
• InjuryJun 15, 2020Malposition of Device; Malposition of Device

  DURING THA SURGERY, IT WAS CONFIRMED BY RADIOGRAPHY THAT TWO SCREWS PENETRATED THE INNER WALL OF THE ACETABULUM. HOWEVER, THE DOCTOR DID NOT MENTION ANYTHING AND THE OPERATION CONTINUED. AFTER THE OPERATION, THE PATIENT COMPLAINED OF PAIN IN THE AFFECTED AREA. THE SCREW THAT HAD PENETRATED MAY HAVE DAMAGED THE NERVE, AND A REVISION WAS PERFORMED IMMEDIATELY. THE LINER AND SCREW WERE REMOVED. ONE SCREW WAS FIXED AGAIN AT A DIFFERENT POSITION. AFTER THE OPERATION, THE PATIENT'S PAIN DISAPPEARED. LEFT SIDE.

  Patient problems: Injury; Pain

  MAUDE report 10152923 ↗
• MalfunctionNov 26, 2019Device Damaged Prior to Use; Device Damaged Prior to Use

  IT WAS REPORTED THAT, DURING A THA, A SURGEON NOTICED A MIS-PROCESSING ON THE SCREW HEAD. A SPARE WAS USED INSTEAD.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9378373 ↗
• InjuryJul 22, 2019Corroded; Corroded

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO LOOSENING OF THE SHELL. INTRA-OPERATIVELY, CORROSION WAS NOTED ON THE SCREWS. THE SHELL, 2 SCREWS AND POLY LINER WERE REVISED. REP REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Injury

  MAUDE report 8811275 ↗
• MalfunctionJun 11, 2019Degraded; Degraded

  6.5MM X 25MM TORX SCREW THREADS STRIPPED. SCREW REMOVED. INSERTED NEW SCREW. NO COMPLICATIONS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8686830 ↗
• MalfunctionApr 3, 2019Particulates; Particulates

  IT WAS REPORTED THAT, DURING A THA, WHEN A SURGEON OPENED THE INNER BLISTER PACKAGE, HE NOTICED A METAL DEBRIS IN THE PACKAGE. A SPARE SCREW WAS USED INSTEAD.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8477844 ↗
• MalfunctionJan 7, 2019Material Separation; Material Separation

  IT WAS REPORTED THAT, DURING A THA, WHEN A NURSE WAS OPENING A OUTER BLISTER PACKAGE, THE TYVEK SHEET WAS DELAMINATED.

  Patient problems: No Patient Involvement

  MAUDE report 8224149 ↗
• InjuryNov 18, 2018Break; Break

  PATIENT CALLED STATING SHE HAD A RIGHT HIP REPLACEMENT ON (B)(6) 2013. PATIENT WAS REVISED ON (B)(6) 2018 DUE TO BROKEN SCREWS. EVENT UPDATE PER MEDICAL REVIEW: ON (B)(6) 2018 A REVISION RIGHT TOTAL HIP ARTHROPLASTY, ACETABULAR COMPONENT AND FEMORAL HEAD, WAS PERFORMED FOR A DIAGNOSIS OF RIGHT THA WITH ACETABULAR LOOSENING. THE OPERATIVE REPORT DESCRIBES SPINAL ANESTHESIA AND USE OF THE PREVIOUS POSTEROLATERAL APPROACH. THE OPERATIVE REPORT NOTES, ¿FEMORAL COMPONENT STABLE, HEAD REMOVED GROSS LOOSENING ACETABULAR COMPONENT REMOVED WITH RELATIVE EASE SCREW BROKEN AND CAME OUT WITH ACETABULAR COMPONENT BONE DEFECT MEDIAL CANCELLOUS BONE GRAFT REAMED FOR A 60 TRIDENT TRITANIUM SHELL WITH FIVE SCREWS, A 36/10° X3 POLY INSERT, A 36/PLUS-2.5 BIOLOX HEAD¿.

  Patient problems: Injury

  MAUDE report 8082775 ↗
• MalfunctionNov 9, 2018Break; Fracture; Break; Fracture

  THE CUSTOMER REPORTED THAT A TRIDENT SCREW BROKE DURING SURGERY WITH THE REMAINDER LEFT IN THE PATIENT. THERE WAS A DELAY OF 5 MINUTES.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8054887 ↗
• InjuryOct 22, 2018Loss of Osseointegration; Loss of Osseointegration

  IT WAS REPORTED BY THE PATIENT AS A RESULT OF A LEGAL CLAIM THAT ALLEGEDLY AFTER THE IMPLANTATION HE DEVELOPED PAIN AND SWELLING WHICH WORSENS AS TIME WENT BY. DURING THE NEXT TWO YEARS BESIDES THE PAIN AND SWELLING THE LEG STARTED TO THUMP WHEN HE WALKED AND SOMETIMES THE HIP WOULD LOCK UP AND COULD NOT MOVE. IT IS FURTHER ALLEGED THAT THE PATIENT WAS REVISED ON (B)(6) 2017 AND DURING THE PROCEDURE THE SURGEON FOUND THAT THE BALL HAD DISINTEGRATED IN THE LEG AND FOUR HOURS WERE SPENT PICKING OUT SHARDS AND SPLINTERS THAT HAD EMBEDDED IN HIS LEG. UPDATE PER MEDICAL REVIEW: ¿ON (B)(6) 2017 HE HAD A LEFT HIP ASPIRATION UNDER LOCAL ANESTHESIA AND FLUOROSCOPIC CONTROL. TOE FLUID WAS SENT FOR GRAM STAIN, CULTURE AND CELL COUNT. LAB REPORT OF RESULTS OF (B)(6) 2017 LEFT HIP ASPIRATE RESULTS: "NO ORGANISMS SEEN" ON GRAM STAIN AND "NO GROWTH AT 3 DAYS" ON CULTURE. CELL COUNT FROM ASPIRATE IS NOT DIAGNOSTIC OF INFECTION.¿ ¿ON (B)(6) 2017 A REVISION LEFT TOTAL HIP ARTHROPLASTY (BOTH COMPONENTS) FOR A PRE­ AND POST-OPERATIVE DIAGNOSIS OF "LEFT HIP PAIN STATUS-POST THA, DISLOCATED LEFT HIP, LOOSENING OF HARDWARE". A BRIEF OPERATIVE REPORT DESCRIBES SPINAL ANESTHESIA AND A LATERAL APPROACH. THE

  Patient problems: Ambulation or Postural Difficulties; Inadequate Osseointegration; Injury; Joint Dislocation; Pain; Swelling

  MAUDE report 7992456 ↗
• MalfunctionOct 2, 2018Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT, DURING A THA, A NURSE WAS OPENING THE OUTER BLISTER PACK, THE TYVEK SHEET WAS DELAMINATED. A SPARE WAS USED INSTEAD.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7926567 ↗
• InjurySep 28, 2018Migration; Migration

  IT WAS REPORTED THROUGH THE SUBMISSION OF A REVISION IMPLANT SHEET THAT PATIENT'S ENTIRE LEFT HIP CONSTRUCT WAS REVISED 16 DAYS AFTER IMPLANTATION. A 52MM CLUSTER HOLE SHELL WITH 2 SCREWS, 36D LINER, 36 -5 CERAMIC HEAD, AND 5X108 STEM WERE REVISED TO A 60MM CLUSTER HOLE SHELL WITH 7 SCREWS, AN ADM/MDM LINER CONSTRUCT, 28 +0 METAL HEAD, AND A 6X111 STEM. UPDATE 31-AUGUST-2018: REP REPORTED THAT PATIENT WAS REVISED DUE TO MOVEMENT OF THE SHELL (DESCRIBED AS HAVING SPUN IN ACETABULUM). SURGEON DECIDED TO IMPLANT A LARGER SHELL AND REVISE THE REST OF THE CONSTRUCT TO SUIT. THERE ARE NO ALLEGATIONS AGAINST THE LINER, HEAD, OR STEM.

  Patient problems: Injury

  MAUDE report 7918323 ↗
• InjurySep 23, 2018Naturally Worn; Naturally Worn

  IT WAS REPORTED THAT:"IT WAS REPORTED THROUGH THE ATTORNEY FOR THE PATIENT, AS A RESULT OF A LAWSUIT, THAT ALLEGEDLY THE PATIENT RECEIVED A TRIDENT CERAMIC ON CERAMIC HIP SYSTEM. IT WAS FURTHER ALLEGED THAT, THE PATIENT BEGAN TO EXPERIENCE SOME DIFFICULTIES, REQUIRING A REVISION SURGERY ON (B)(6) 2008." UPDATE AS PER MEDICAL REVIEW: "ON (B)(6) 2008 A REVISION OF THE RIGHT TOTAL HIP WAS PERFORMED WITH REMOVAL OF LOOSE, FRACTURED CERAMIC PIECES. EXTENSIVE METALLOSIS WAS NOTED AND A REVISION TOTAL HIP WAS PERFORMED FOR A DIAGNOSIS OF FRACTURED CERAMIC HEAD AND LINER, DISPLACED METAL LINER, EROSION SUPERIOR ACETABULAR SHELL, AND EXTENSIVE WEAR DEBRIS."

  Patient problems: Device Embedded In Tissue or Plaque; Inflammation; Injury; Reaction

  MAUDE report 7900661 ↗
• MalfunctionSep 19, 2018Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT, DURING A THA, WHEN A NURSE WAS OPENING THE BLISTER PACKAGE, THE TYVEK SHEET WAS DELAMINATED. A SPARE WAS USED INSTEAD.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7890080 ↗
• MalfunctionJul 20, 2018Packaging Problem; Packaging Problem

  ONLY SINGLE LAYER DISINFECTANT PACKAGE. THE PACKAGE WAS MISSING THE INNER BLISTER.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7707791 ↗
• MalfunctionJul 19, 2018Packaging Problem; Packaging Problem

  ONLY SINGLE LAYER DISINFECTANT PACKAGE. THE PACKAGE WAS MISSING THE INNER BLISTER.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7704337 ↗
• InjuryJul 10, 2018Break; Crack; Fracture; Break; Crack; Fracture

  IT WAS REPORTED THAT SURGEON REVISED PATIENT'S RIGHT HIP DUE TO A LOOSE CUP. SURGEON REVISED CUP, LINER HEAD AND SLEEVE. POSTOPERATIVE DIAGNOSIS: PATIENT UNDERWENT REVISION OF PRIMARY RIGHT THA (B)(6) 2015 FOR METALLOSIS. PATIENT UNDERWENT SUBSEQUENT REVISION OF ACETABULAR COMPONENT (B)(6) 2015. UPDATE AS PER MEDICAL REVIEW: ..."THE OVERLOAD CONDITION COULD CONTINUE ITS DETRIMENTAL EFFECTS AND CAUSED PERSISTING PAIN PROBLEMS IMMEDIATELY AFTER THE FIRST REVISION AND CONTINUING UNTIL CATASTROPHIC CUP FAILURE WITH LOOSENING, SCREW FRACTURE AND SEVERE BONE LOSS REQUIRING AN EXTENSIVE SECOND REVISION SURGERY." SUBOPTIMAL CUP POSITION REGARDING INCLINATION AND ANTEVERSION HAS CONTRIBUTED TO OVERLOAD IN THE CUP SHELL CONTRIBUTING TO LOSS OF FIXATION IN THE CUP SHELL AND CONSEQUENT OVERLOAD ON THE SUPPLEMENTAL CUP FIXATION SCREWS. OSTEOLYSIS DEVELOPED AROUND THE SCREW AREA CAUSING OSTEOLYTIC GRANULOMA FORMATION AS SOFT TISSUE MASS IN THE PELVIS. DURING THE FIRST REVISION THE PROBLEM WAS NOT RECOGNIZED WITH ONLY BEARING EXCHANGE AND THUS THE CONDITION FURTHER DETERIORATED UNTIL CATASTROPHIC CUP FIXATION FAILURE WITH SCREW FRACTURE ONLY 9-MONTHS LATER REQUIRING A SECOND REVISION.

  Patient problems: Injury; Osteolysis

  MAUDE report 7674624 ↗
• InjuryJun 28, 2018Break; Fracture; Loss of Osseointegration; Break; Fracture; Loss of Osseointegration

  IT WAS REPORTED BY THE ATTORNEY, THROUGH THE FILING OF A LAWSUIT, THAT THE PLAINTIFF UNDERWENT A RIGHT TOTAL HIP ARTHROPLASTY ON (B)(6) 2015 WHERE SHE WAS IMPLANTED WITH A STRYKER SECUR-FIT MAX SYSTEM. IT IS FURTHER ALLEGED THAT "IN THE SPRING OF 2016, PLAINTIFF BEGAN EXPERIENCING EXTREME PAIN AND DISCOMFORT IN HER LOWER BACK AND RIGHT HIP. SHE HAD DIFFICULTY WALKING AND REQUIRED THE USE OF A CRUTCH TO GET AROUND". THE PATIENT'S RIGHT HIP WAS THEN REVISED ON (B)(6) 2016. DR. (B)(6) STATED IN HIS OPERATIVE REPORT THAT "ONE OF THE SCREW HEAD [SIC] WAS BROKEN AND WAS REMOVED AND THEN THE CUP REMOVED". DR. (B)(6) ALSO NOTED THAT AN "ADDITIONAL BROKEN SCREW WAS REMOVED USING HAND INSTRUMENTS".

  Patient problems: Ambulation or Postural Difficulties; Discomfort; Inadequate Osseointegration; Injury; Pain

  MAUDE report 7645761 ↗
• InjuryJun 25, 2018Break; Fracture; Break; Fracture

  IT WAS REPORTED BY THE ATTORNEY, THROUGH THE FILING OF A LEGAL CLAIM, THAT THE PATIENT UNDERWENT A RIGHT TOTAL HIP ARTHROPLASTY ON (B)(6) 2011 WHERE SHE WAS IMPLANTED WITH A STRYKER HIP SYSTEM. IT IS FURTHER ALLEGED THAT THE PATIENT BEGAN EXPERIENCING RIGHT HIP PAIN AND WAS USING A WALKER FOR AMBULATION. X-RAYS TAKEN IN 2016 "REVEALED A BROKEN SCREW WITHIN THE ACETABULAR COMPONENT AND MEDIAL MIGRATION OF THE ACETABULAR COMPONENT CAUSING PROTRUSION". THE PATIENT THEN UNDERWENT REVISION SURGERY OF THE RIGHT HIP ACETABULAR COMPONENT ON (B)(6) 2017.

  Patient problems: Ambulation or Postural Difficulties; Injury; Pain

  MAUDE report 7635448 ↗
• MalfunctionApr 18, 2018Device Damaged Prior to Receipt by User; Tear, Rip or Hole in Device Packaging; Device Damaged Prior to Receipt by User; Tear, Rip or Hole in Device Packaging

  AS REPORTED: "THE SCREW BOX LOOKS TO HAVE BEEN SMASHED DURING DELIVERY AND CAUSED THE THREADS OF THE SCREW TO PUSH THROUGH THE PACKAGING."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7440257 ↗
• MalfunctionMar 2, 2018Packaging Problem; Packaging Problem

  PRIMARY PROCEDURE, RIGHT HIP. REP WAS PRESENT IN THE OPERATING ROOM. IT WAS REPORTED THAT A 25 MM SCREW WAS REQUESTED. REP HANDED A BOX MARKED FOR A 25 MM SCREW TO THE NURSE. THE NURSE TOOK THE INNER PACKAGING OUT, OPENED IT, AND HANDED THE SCREW TO THE SURGEON. NURSE VERIFIED THAT THE INNER PACKAGING WAS MARKED FOR A 20 MM SCREW. BY THIS TIME, THE SCREW WAS INSIDE THE PATIENT. SURGEON REPORTED HE HAD FELT THE SCREW WAS SHORTER THAN EXPECTED. NO SURGICAL DELAY WAS CAUSED AS THE SCREW WENT DIRECTLY INTO THE PATIENT, AND SURGEON REPORTED SATISFACTORY FIXATION AND NO PATIENT HARM DUE TO THE SHORTER SCREW.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7309434 ↗
• MalfunctionNov 30, 2017Device Operates Differently Than Expected; Device Operates Differently Than Expected

  SALES REP REPORTED, DURING PRIMARY HIP SURGERY SURGEON HAD DIFFICULTY GETTING THREE SCREWS TO GO IN CUP; SURGEON OPENED NEW SCREWS TO COMPLETE SURGERY. THERE WAS A 15 - 20 MINUTE DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7071766 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K873251, K894124. One submission often covers many models, so check the product and lot details in each record.

• Z-0483-2014 · Oct 1, 2013 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker France Both the 6.4 mm diameter, 25mm length, Cancellous Bone Screws (Cat no 2030-6525-1) and the 5.5
• Z-0388-2013 · Aug 17, 2012 · Terminated
  Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw Ref 2030-6535-1 The 6.5mm Cancellous Bone Screws are used in THA when the surgeon elects to use a cluster/multi-hole shell i
• Z-0387-2013 · Aug 17, 2012 · Terminated
  Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw Ref 2030-6525-1 The 6.5mm Cancellous Bone Screws are used in THA when the surgeon elects to use a cluster/multi-hole shell i
• Z-2143-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Restoration Gap Plate Screw; Dia. 6.5 mm, Lnth 60 mm; Made in USA, Sterile; Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430
• Z-2135-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Restoration Gap Plate Screw; Dia. 6.5 mm, Lnth 20 mm; Made in USA, Sterile; Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430
• Z-2141-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Restoration Gap Plate Screw; Dia. 6.5 mm, Lnth 50 mm; Made in USA, Sterile; Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430
• Z-2121-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 40 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are op
• Z-2142-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Restoration Gap Plate Screw; Dia. 6.5 mm, Lnth 55 mm; Made in USA, Sterile; Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430
• Z-2120-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 30 mm; Sterile; Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are op
• Z-2130-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw; Dia 5.5 mm; Lnth: 40 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are op
• Z-2140-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Restoration Gap Plate Screw; Dia. 6.5 mm, Lnth 45 mm; Made in USA, Sterile; Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430
• Z-2119-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 25 mm; Sterile; Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are op
• Z-2176-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 35 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are op
• Z-2127-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw; Dia 5.5 mm; Lnth: 25 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are op
• Z-2123-2009 · Jun 26, 2009 · Terminated
  Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 50 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are op

…and 17 more.