510(k) K103124 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
SERIES II X3 LARGE DIAMETER ACCETABULAR INSERTS
| Applicant | Stryker Corporation, Mahwah NJ, US |
| Decision | Substantially Equivalent, Nov 19, 2010 |
| Received | Oct 22, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103124
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.