510(k) K030501 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
X-SERIES INTEGRAL LATERALIZED HIP COMPONENTS
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Mar 20, 2003 |
| Received | Feb 19, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030501
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.