510(k) K171365 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Arthrex Knee Systems
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Nov 7, 2017 |
| Received | May 9, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171365
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.