510(k) K093533 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0
| Applicant | Materialise NV, Leuven, BE |
| Decision | Substantially Equivalent, Feb 17, 2010 |
| Received | Nov 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093533
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.