510(k) K130573 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
TYBER MEDICAL INTERBODY SYSTEM; ACIF, ALIF, PLIF, TLIF, DLIF
| Applicant | Tyber Medical, LLC, Morristown NJ, US |
| Decision | Substantially Equivalent, Sep 30, 2013 |
| Received | Mar 4, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130573
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.