510(k) K090060 ยท KWP Appliance, Fixation, Spinal Interlaminal
NEXLINK OCT SYSTEM, MODEL 7000 SERIES
| Applicant | Abbott Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Jun 2, 2009 |
| Received | Jan 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090060
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.