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Medtronic Reusable Instruments

MEDTRONIC SOFAMOR DANEK, INC. · Model X0805152 · UDI-DI 00613994167484

KIL Prescription
1
510(k) clearances
11
Adverse events
0
Recalls
36
Facilities

Description

INSTRUMENT X0805152 6.35 MAS HEAD POSTNR

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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.