510(k) K090316 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO: LANX ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Lanx, Inc., Broomfield CO, US |
| Decision | Substantially Equivalent, Apr 7, 2009 |
| Received | Feb 9, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090316
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.