SUPER QUICKANCHOR PLUS— 510(k) K041116

Substantially Equivalent

Depuy Mitek

FDA 510(k) clearance K041116 for SUPER QUICKANCHOR PLUS, Substantially Equivalent on 2004-05-28. Applicant: Depuy Mitek.

Clearance details

Applicant: Depuy Mitek
Product code: Code JDR
Advisory panel: Orthopedic
Date received: 2004-04-29
Decision date: 2004-05-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Norwood, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code JDR

product code JDR

Injury: 726
Malfunction: 663
Other: 1
Total: 1,390

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.