K020948

Substantially Equivalent

SMITH & NEPHEW SURETAC - EXPANDED INDICATIONS II

Applicant: Smith & Nephew, Inc.
Product code: JDR
Advisory panel: Orthopedic
Date received: 2002-03-25
Decision date: 2002-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

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.