Intervertebral fusion device with bone graft, lumbar

FDA product code MAX · Class 2 · 1,241 devices · 3,549 reports · 5 deaths reported · 316 devices named in recalls

• Aero-LL 48941310

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48951086

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48951136

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48952080

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48953070

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48953080

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48954086

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48955136

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48955166

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48956106

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48956136

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48956112

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48953092

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48953142

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium PL 48956116

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium TL 48932092

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Tritanium TL 48930106

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Monterey AL 480110531

  Stryker Corporation · Intervertebral fusion device with bone graft, lumbar
  1 report
• Mectalif Oblique Cages 03.20.052

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Transforaminal Cages 03.23.053

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Transforaminal Cages 03.23.056

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Transforaminal Cages TiPEEK 03.23.151

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Transforaminal Cages TiPEEK 03.23.153

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Transforaminal Cages TiPEEK 03.23.154

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Oblique 03.26.017

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Oblique 03.26.034

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Oblique 03.26.085

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Posterior 03.27.001

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Posterior 03.27.008

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Posterior 03.27.020

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Posterior 03.27.044

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Posterior Cages 03.27.113

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Posterior Cages 03.27.114

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Mectalif Posterior Cages 03.27.139

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• MectaLIF 3D 03.41.057

  Medacta International SA · Intervertebral fusion device with bone graft, lumbar
  1 report
• MectaLIF 03.26.306

  Medacta International SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• JULIET INSTRUMENTATION JUL-IO 00 01-N

  SpineArt SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• JULIET ® Ti PO JUT-P6 24 11-S

  SpineArt SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• JULIET ® Ti LL JLT-MX 50 14-S

  SpineArt SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• SCARLET® AL-T Intervertebral body fusion device SCA-LS 15 12-S

  SpineArt SA · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Kleiner KG2 system KG2 Static Lordotic 11x28x13x6°

  Baat Medical Products B.V. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Pulsar Expandable PLIF System 2210-0941

  GS Medical Co., Ltd. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• LnK Lumbar Interbody Fusion Cage System 3810-5010

  L&K Biomed CO. ,Ltd. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• CONCORDE 187823110

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE 187823410

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE 187827110

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE 187827411

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE 187831209

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE 187850208

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189150508

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189150510

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189155510

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189155512

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189155514

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189160508

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189160510

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189145614

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• COUGAR 189155614

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE 196923511

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE 196923011

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE LIFT 2878-80-117

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE LIFT 1978-11-021C

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONCORDE LIFT 1978-11-027L

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT AET10210T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT AET10208T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT LET30100T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT LET30200T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT TFT80932T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT PET21010T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT PET20910T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT PET30200T

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• CONDUIT 187210310

  Medos International Sàrl · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 08.812.008

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 08.812.012

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 08.812.209

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 08.812.211

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 08.812.213

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• SynCage 08.825.111S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• SynCage 08.825.224S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• SynCage 08.825.265S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• SynCage 08.825.323S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 04.812.217S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 04.812.015S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 04.812.212S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 04.812.012S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 04.812.013S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• T-PAL 04.812.213S

  Synthes GmbH · Intervertebral fusion device with bone graft, lumbar
  1 report
• Leva™ Spacer System 11-7012

  Spine Wave, Inc. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Leva® Spacer System 11-7023

  Spine Wave, Inc. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• Leva® Spacer System 11-7223

  Spine Wave, Inc. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• True Position® Spacer System 1208-01-2709

  Spine Wave, Inc. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• True Position® Spacer System 1208-01-3010

  Spine Wave, Inc. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• True Position® Spacer System 1208-01-3011

  Spine Wave, Inc. · Intervertebral Fusion Device With Bone Graft, Lumbar
  1 report
• ALEUTIAN® Interbody Systems 3303-20728M

  VB Spine LLC · Intervertebral fusion device with bone graft, lumbar
  1 report
• ALEUTIAN® Interbody Systems 5203-20428L6

  VB Spine LLC · Intervertebral fusion device with bone graft, lumbar
  1 report
• ALEUTIAN® Interbody Systems 602-90777

  VB Spine LLC · Intervertebral fusion device with bone graft, lumbar
  1 report
• ALEUTIAN® Interbody Systems 603-20728C

  VB Spine LLC · Intervertebral fusion device with bone graft, lumbar
  1 report
• CASCADIA™ Interbody System 6101-2102808TL7-G2

  VB Spine LLC · Intervertebral fusion device with bone graft, lumbar
  1 report
• CASCADIA™ Interbody System 6101-2102812TL7-G2

  VB Spine LLC · Intervertebral fusion device with bone graft, lumbar
  1 report
• CASCADIA™ Interbody System 6101-2102814NC-G2

  VB Spine LLC · Intervertebral fusion device with bone graft, lumbar
  1 report