510(k) K991873 ยท HRS Plate, Fixation, Bone
KMI WRIST FUSION SYSTEM
| Applicant | Kinetikos Medical, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 17, 1999 |
| Received | Jun 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991873
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.