510(k) K013683 ยท GAW Suture, Nonabsorbable, Synthetic, Polypropylene
MODIFICATION TO: ABBOTT VASCULAR SUTURE ANASTOMOSIS DEVICE
| Applicant | Abbott Vascular, Inc., Redwood CA, US |
| Decision | Substantially Equivalent, Dec 6, 2001 |
| Received | Nov 7, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013683
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.