510(k) K050699 ยท JDK Prosthesis, Hip, Cement Restrictor
MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004
| Applicant | Amedica Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Apr 15, 2005 |
| Received | Mar 18, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050699
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.