510(k) K080685 ยท JDO Device, Fixation, Proximal Femoral, Implant
HIPLOC COMPRESSION HIP SCREW
| Applicant | Biomet Manufacturing, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 15, 2008 |
| Received | Mar 11, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080685
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 9, 2018 | Biomet UK Ltd. HipLOC Hip Fracture Fixation System- Hiploc System 130 Plate 38 mm Barrel 4 Hole Plate
Item Number: 2110-130-004
Product Usage:
The HipLOC Compression Hip Screw may be used primarily for fixation of Terminated |
JDO | None listed |
| Aug 9, 2018 | Biomet UK Ltd. HipLOC Hip Fracture Fixation System-Hiploc System 135 Plate 38 mm Barrel 3 Hole Plate
Item Number: 2110-135-003
Product Usage:
The HipLOC Compression Hip Screw may be used primarily for fixation of Terminated |
JDO | None listed |
| Aug 9, 2018 | Biomet UK Ltd. HipLOC Hip Fracture Fixation System-Hiploc System 135 Plate 38 mm Barrel 4 Hole Plate
Item Number: 2110-135-004
Product Usage:
The HipLOC Compression Hip Screw may be used primarily for fixation of b Terminated |
JDO | None listed |
| Aug 9, 2018 | Biomet UK Ltd. HipLOC Hip Fracture Fixation System-Hiploc System 140 Plate 38 mm Barrel 4 Hole Plate
Item Number: 2110-140-004
Product Usage:
The HipLOC Compression Hip Screw may be used primarily for fixation of Terminated |
JDO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.