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Intercept™
MEDTRONIC, INC. · Model 37441-RFB · UDI-DI 00763000875602
MBX
Prescription
0
510(k) clearances
403
Adverse events (2 deaths)
0
Recalls
11
Facilities
Description
PROG 37441 INTERCEPT DBS REFURB US
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.