510(k) K141920 ยท KWN Prosthesis, Wrist, Carpal Lunate
Wrist Hemiarthroplasty System
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Dec 23, 2014 |
| Received | Jul 16, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141920
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.