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MEDTRONIC, INC. · Model 3708660 · UDI-DI 00763000236830

PJSOLMMHYNHLMRUMBX Prescription
0
510(k) clearances
2,224
Adverse events (5 deaths)
0
Recalls
29
Facilities

Description

EXT 3708660 DBS US 60CM EMANUAL EN

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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.