510(k) K020056 ยท HWC Screw, Fixation, Bone
DUET SUTURE ANCHOR
| Applicant | Bionx Implants, Ltd., Tampere, FI |
| Decision | Substantially Equivalent, Jun 26, 2002 |
| Received | Jan 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020056
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.