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General Instruments
ALPHATEC SPINE, INC. · Model CI-10961 · UDI-DI 00840180508336
HYA
Prescription
0
510(k) clearances
11
Adverse events (1 deaths)
1
Recalls
105
Facilities
Description
Passive Lock Wire Slap Hammer
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-06-17 | Biomet, Inc. | Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.