510(k) K943804 ยท HWC Screw, Fixation, Bone
BONE SCREW
| Applicant | Cohort Medical Products Group, Inc., Hayward CA, US |
| Decision | Substantially Equivalent for Some Indications, Dec 8, 1994 |
| Received | Aug 4, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943804
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.