510(k) K143572 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Intersomatic Cervical Device - DICOM PEEK, Intersomatic Intervertebral Space Maintenance Device - DIMEI PEEK, Intersomatic Transforaminal - TLIF PEEK
| Applicant | Osteomed Implantes, Ltda, Rio Claro - Sp, BR |
| Decision | Substantially Equivalent, Jun 10, 2015 |
| Received | Dec 17, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143572
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.