510(k) K101364 ยท MRW System, Facet Screw Spinal Device
LANX FACET SCREW SYSTEM
| Applicant | Lanx, Inc., Broomfield CO, US |
| Decision | Substantially Equivalent, Aug 16, 2010 |
| Received | May 14, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101364
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.