510(k) K021919 ยท KWP Appliance, Fixation, Spinal Interlaminal
SCS CLARIS SPINAL SYSTEM,REXTENDED OMNIAXIAL CONNECTOR-,MEDIUM, MODEL CO05, SCS CLARIS SPINAL SYSTEM,EXTENDED OMNIAXIALO
| Applicant | Ortho Tec, LLC, Chesterland OH, US |
| Decision | Substantially Equivalent, Jul 3, 2002 |
| Received | Jun 11, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021919
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.