510(k) K933719 ยท HWC Screw, Fixation, Bone
BIOSCREW ABSORBABLE INTERFERENCE SCREW
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent for Some Indications, May 17, 1994 |
| Received | Aug 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933719
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.