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LEVEL ONE
KLS-Martin L.P. · Model 50-502-12-07 · UDI-DI 00888118077141
HXZ
Prescription
1
510(k) clearances
514
Adverse events
1
Recalls
247
Facilities
Description
CUTTER, MESH, HEAVY, W/LONG CUTTING INSERT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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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.