510(k) K212038 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage
| Applicant | K&J Consulting Corporation, Lansdale PA, US |
| Decision | Substantially Equivalent, Aug 27, 2021 |
| Received | Jun 30, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212038
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.