510(k) K052638 ยท KNW Instrument, Biopsy
ABBOTT SPINE, INC. SPINNAKER SYSTEM
| Applicant | Abbott Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Nov 7, 2005 |
| Received | Sep 26, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052638
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.