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NeuroPro® Low Profile
Kinamed, Inc. · Model 16-1S1-2004 · UDI-DI 00898142001807
7
510(k) clearances
81
Adverse events
1
Recalls
35
Facilities
Description
Bone Screw, 2.0 x 4mm
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.