FDA Device Intelligence
Home › MEDTRONIC, INC. › InterStim™ SureScan™

InterStim™ SureScan™

MEDTRONIC, INC. · Model 978A133 · UDI-DI 00763000913083

QONEZW Prescription
0
510(k) clearances
10
Adverse events
0
Recalls
19
Facilities

Description

LEAD 978A133 ISTM 2.16MM EMAN EUMDR LI08

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.