510(k) K041749 ยท HWC Screw, Fixation, Bone
SCANDIUS ACL RECONSTRUCTION SYSTEM
| Applicant | Scandius Biomedical, Inc., Littleton MA, US |
| Decision | Substantially Equivalent, Sep 8, 2004 |
| Received | Jun 29, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041749
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.