510(k) K990523 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
B2C, ESPACE REVISION CUP SYSTEM
| Applicant | Turnkey Intergration USA, Inc., Sarasota FL, US |
| Decision | Substantially Equivalent, Apr 30, 1999 |
| Received | Feb 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990523
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.