510(k) K073177 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, May 13, 2008 |
| Received | Nov 13, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K073177
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 3, 2014 | RTI Surgical, Inc. C-Plus" 10mm x 12mm Webless implants
Pioneer Surgical's C-Plus " 10mm x 12mm Webless implants are cervical intervertebral fusion devices that are intended to stabilize a cervical spinal segment to pr Terminated |
ODP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.