510(k) K101812 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CONSTRUX MINI PEEK SPACER SYSTEM
| Applicant | Orthofix, Inc., Mckinney TX, US |
| Decision | Substantially Equivalent, Sep 27, 2010 |
| Received | Jun 29, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101812
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.