MODIFIED ENDO STICH— 510(k) K082659

Substantially Equivalent

Covidien Lp, Formerly Registered AS United States

FDA 510(k) clearance K082659 for MODIFIED ENDO STICH, Substantially Equivalent on 2008-09-19. Applicant: Covidien Lp, Formerly Registered AS United States.

Clearance details

Applicant: Covidien Lp, Formerly Registered AS United States
Product code: Code OCW
Advisory panel: Gastroenterology, Urology
Date received: 2008-09-12
Decision date: 2008-09-19
Decision: Substantially Equivalent
Clearance type: Special
Location: North Haven, CT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OCW

product code OCW

Death: 6
Injury: 443
Malfunction: 1,023
Other: 2
Total: 1,474

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.