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AXS
Stryker Leibinger GmbH & Co. KG · Model 56-15933S4 · UDI-DI 37613327357166
HBW
Prescription
1
510(k) clearances
81
Adverse events
1
Recalls
35
Facilities
Description
SCREW, AXS, SELF-DRILLING
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-01-24 | Synthes (USA) Products LLC | Products not sterilized, sterility cannot be confirmed |
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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.