510(k) K192054 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Endoskeleton TAS Plate
| Applicant | Titan Spine, Inc., Mequon WI, US |
| Decision | Substantially Equivalent, Aug 29, 2019 |
| Received | Jul 31, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192054
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.