510(k) K082991 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
BIOLOX DELTA CERAMIC FEMORAL HEAD
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Nov 20, 2008 |
| Received | Oct 7, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082991
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.