510(k) K101765 ยท MRW System, Facet Screw Spinal Device
KYPHON ANCHOR FACET SCREW SYSTEM
| Applicant | Medtronic Spine, LLC, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Oct 22, 2010 |
| Received | Jun 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101765
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.