510(k) K000321 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
HEMISPHERE MODULAR CUP SYSTEM
| Applicant | Ortho Development Corp., Draper UT, US |
| Decision | Substantially Equivalent, Apr 10, 2000 |
| Received | Feb 2, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000321
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.