510(k) K071633 ยท KWP Appliance, Fixation, Spinal Interlaminal
LANX DEFORMITY SYSTEM
| Applicant | Lanx, LLC, Philadelphia PA, US |
| Decision | Substantially Equivalent, Aug 15, 2007 |
| Received | Jun 14, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071633
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.