510(k) K960533 ยท HWC Screw, Fixation, Bone
K3 BONE SCREW SYSTEM
| Applicant | Kinetikos Medical, Inc., San Diego CA, US |
| Decision | Substantially Equivalent for Some Indications, Mar 25, 1996 |
| Received | Feb 7, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960533
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.