PROSTIVA RF THERAPY HAND PIECE, MODEL 8929— 510(k) K082464

Substantially Equivalent

Medtronic, Inc.

FDA 510(k) clearance K082464 for PROSTIVA RF THERAPY HAND PIECE, MODEL 8929, Substantially Equivalent on 2008-10-27. Applicant: Medtronic, Inc..

Clearance details

Applicant: Medtronic, Inc.
Product code: Code KNS
Advisory panel: Gastroenterology, Urology
Date received: 2008-08-27
Decision date: 2008-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KNS

product code KNS

Death: 44
Injury: 2,361
Malfunction: 4,771
Total: 7,176

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.