510(k) K081172 ยท JDR Staple, Fixation, Bone
COMPOSITE HITCH SUTURE ANCHOR
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 17, 2008 |
| Received | Apr 24, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081172
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.