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OsteoMed
OSTEOMED LLC · Model 114-2051 · UDI-DI 00842528114292
GXL
Prescription
0
510(k) clearances
16
Adverse events
2
Recalls
17
Facilities
Description
2.0MM DRIVER STEM W/POST, AO SHNK, MED
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-01-30 | Synthes, Inc. | The CMF Battery Powered Driver graphic case contains outlines of the Battery Powered Driver, taps, screwdriver blades, and a screw holding sleeve. However, the device is not inten |
| 2006-03-08 | Medtronic Neurosurgery | Medtronic Neurosurgery has initiated this action because it was determined that two lots of the Modular Screwdriver Blade components may exhiibt burrs along the tips of the Screwd |
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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.