510(k) K161809 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ShurFit CpTi-HA ACIF Interbody Fusion System
| Applicant | Precision Spine, Inc., Pear MS, US |
| Decision | Substantially Equivalent, Dec 6, 2016 |
| Received | Jul 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161809
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.