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Medtronic Reusable Instruments

MEDTRONIC SOFAMOR DANEK, INC. · Model X1100018 · UDI-DI 00681490614528

HWK Prescription
1
510(k) clearances
132
Adverse events
0
Recalls
127
Facilities

Description

20 X 80MM DISCECTOMU BLADE

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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.