510(k) K113800 ยท GAW Suture, Nonabsorbable, Synthetic, Polypropylene
QUILL QUADRAHELIX TISSUE-CLOSURE DEVICE
| Applicant | Angiotech, Reading PA, US |
| Decision | Substantially Equivalent, Jan 20, 2012 |
| Received | Dec 23, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113800
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.