K961578

Substantially Equivalent

SUTURE ANCHOR

Applicant: United States Surgical, A Division of Tyco Healthc
Product code: JDR
Advisory panel: Orthopedic
Date received: 1996-04-24
Decision date: 1996-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, 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.