510(k) K132312 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
RENOVIS TESERA TRABECULAR TECHNOLOGY (T3) ACETABULAR SHELL SYSTEM
| Applicant | Renovis Surgical Technologies, LLC, Ashland MA, US |
| Decision | Substantially Equivalent, Apr 11, 2014 |
| Received | Jul 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132312
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.