510(k) K060081 ยท KWP Appliance, Fixation, Spinal Interlaminal
BASIS SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Feb 13, 2006 |
| Received | Jan 10, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060081
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.