510(k) K103491 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SKYLINE ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | A Johnson & Johnson Company, Raynham MA, US |
| Decision | Substantially Equivalent, Feb 14, 2011 |
| Received | Nov 26, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103491
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.