510(k) K052630 ยท HWC Screw, Fixation, Bone
ROTATOR CUFF QUICKANCHOR PLUS (WITH ORTHOCORD SUTURE)
| Applicant | Depuy Mitek, A Johnson & Johnson Company, Norwood MA, US |
| Decision | Substantially Equivalent, Oct 17, 2005 |
| Received | Sep 26, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052630
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.