510(k) K971206 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
MERIDIAN ST FEMORAL STEM AND VITALOCK SOLID BACK SHELL W/ PERI-APATITE COATING
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent for Some Indications, Feb 11, 1998 |
| Received | Mar 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971206
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 1, 2005 | Stryker Howmedica Osteonics Corp. Meridian ST Femoral Stem Terminated |
MAY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.