510(k) K071377 ยท KWP Appliance, Fixation, Spinal Interlaminal
POLARIS BE RODS
| Applicant | Biomet Spine, Parsippany NJ, US |
| Decision | Substantially Equivalent, Aug 6, 2007 |
| Received | May 17, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071377
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.