510(k) K003823 ยท KWP Appliance, Fixation, Spinal Interlaminal
SCS DT-02 TRANSVERSE CONNECTOR
| Applicant | Ortho Tec, LLC, Beverly Hills CA, US |
| Decision | Substantially Equivalent, Jul 11, 2001 |
| Received | Dec 11, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003823
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.