510(k) K163269 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device
| Applicant | Titan Spine, LLC, Mequon WI, US |
| Decision | Substantially Equivalent, Apr 13, 2017 |
| Received | Nov 21, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163269
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.