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APTUS

Medartis AG · Model A-5800.22 · UDI-DI 07630037883357

HWC Prescription
1
510(k) clearances
58,942
Adverse events (75 deaths)
0
Recalls
657
Facilities

Description

2.8 Cortical Screw 22mm, HD7, 5/Pkg

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.