510(k) K980020 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
ACTIVELOCK MODULAR FEMORAL HIP SYSTEM
| Applicant | Metagen, LLC, San Diego CA, US |
| Decision | Substantially Equivalent for Some Indications, Apr 3, 1998 |
| Received | Jan 5, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980020
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.