510(k) K113829 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ZIMMER PATIENT SPECIFIC INSTRUMENT SYSTEM ZIMMER PATIENT SPECIFIC INSTRUMENTS ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNE
| Applicant | Materialise NV, Leuven, BE |
| Decision | Substantially Equivalent, Apr 2, 2012 |
| Received | Dec 27, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113829
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.