510(k) K131474 ยท HRS Plate, Fixation, Bone
ARTHREX DISTAL RADIUS PLATE SYSTEM
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jul 3, 2013 |
| Received | May 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131474
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.