510(k) K092110 ยท HSB Rod, Fixation, Intramedullary And Accessories
WAVEON FRACTURE REPAIR SYSTEM (WAVEON RX)
| Applicant | Sonoma Orthopedic Products, Inc., Santa Rosa CA, US |
| Decision | Substantially Equivalent, Jan 20, 2010 |
| Received | Jul 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092110
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.