510(k) K191621 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ChoiceSpine Octane A/T/P Spinal Implant System, ChoiceSpine Cervical Interbody Spacer System Ascendant PC, ChoiceSpine Cervical Interbody Spacer System Ascendant, ChoiceSpine Cervical Spacer System Blackhawk, ChoiceSpine Intervertebral Fusion Device Octane Straight, ChoiceSpine Intervertebral Fusion
| Applicant | Choice Spine, LLC, Knoxville TN, US |
| Decision | Substantially Equivalent, Aug 15, 2019 |
| Received | Jun 18, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191621
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.