Camber 8370013PRecalls & reported problems
Nuvasive, Inc. · Camber Traditional Plate, 8mm C-C · Class 2 · Implant
- 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 00887517995704), received between Aug 23, 2024 and Aug 23, 2024 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Vertebral Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON (B)(6) A PATIENT UNDERWENT A CERVICAL FUSION PROCEDURE FROM C4-C6. DURING THE PROCEDURE THE HINGE SIDE OF THE C6 BONE WAS FRACTURED WHEN THE CAMBER PLATE WAS PLACED AT C6. IT IS UNKNOWN WHETHER THE PATIENT WAS EXPERIENCING ANY ADDITIONAL ADVERSE CONSEQUENCES AS A RESULT OF THE VERTEBRAL FRACTURE. IT IS UNKNOW WHAT WAS DONE TO TREAT/ADDRESS THE VERTEBRAL FRACTURE.
Patient problems: Vertebral Fracture
MAUDE report 20057555 ↗
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
- Centerpiece Plate Fixation System G8532067Medtronic Sofamor Danek, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL3 reports
- Xspan Laminoplasty Fixation System X085-0150-STRXtant Medical Holdings, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL3 reports
- ESCALATE 48570300Stryker Corporation · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL2 reports
- Gallery™ Laminoplasty System 14-523101Biomet Spine LLC · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL1 report
- Gallery™ Laminoplasty System 14-523100Biomet Spine LLC · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.