510(k) K103393 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
POLARIS SPINAL SYSTEM
| Applicant | Biomet Spine, Parsippany NJ, US |
| Decision | Substantially Equivalent, Feb 2, 2011 |
| Received | Nov 19, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103393
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.