CENTERPIECE™ Plate Fixation System 853010WMRecalls & reported problems
Medtronic Sofamor Danek, Inc. · PLATE 853010WM OD WIDE MOUTH 10MM · Class 2 · Implant
All models of Centerpiece Plate Fixation System (5)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885074317458), received between Jan 18, 2017 and Jan 18, 2017 — classified as 1 injury.
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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Muscle Weakness/Atrophy1
- Neck Pain1
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 18, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON (B)(6) 2016, PATIENT UNDERWENT A SURGERY DUE TO OSSIFICATION OF POSTERIOR LONGITUDINAL LIGAMENT AND STENOSIS OF SPINAL CANAL. POST-OP, PATIENT HAD NECK PAIN, LIMB WEAKNESS AND 0 LOWER LIMB MUSCLE STRENGTH. DUE TO WHICH THE PATIENT UNDERWENT A REVISION SURGERY ON (B)(6) 2016 IN WHICH POSTERIOR CERVICAL DECOMPRESSION WITH VERTEX INTERNAL FIXATION WAS PERFORMED. THE PRODUCTS CAME IN CONTACT WITH THE PATIENT. PATIENT WAS ALSO REPORTED WITH BLEEDING "AFTER THE SURGERY." AFTER REVISION SURGERY PATIENT HAD NECK PAIN RELIEF BUT 0 LOWER LIMB MUSCLE STRENGTH.
Patient problems: Muscle Weakness/Atrophy; Neck Pain; No Code Available
MAUDE report 6259504 ↗
Other ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL devices
- Centerpiece Plate Fixation System 8532065Medtronic Sofamor Danek, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL13 reports
- Centerpiece Plate Fixation System 8532067Medtronic Sofamor Danek, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL11 reports
- Xspan Laminoplasty Fixation System X085-0250-STRXtant Medical Holdings, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL6 reports
- Xspan Laminoplasty Fixation System X085-0150-STRXtant Medical Holdings, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL3 reports
- Centerpiece Plate Fixation System G8532067Medtronic Sofamor Danek, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL3 reports
- ESCALATE 48570300Stryker Corporation · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL2 reports
- CANOPY 1102.1005Globus Medical, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL1 report
- CANOPY 1102.4011Globus Medical, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page