SUTURE ANCHOR— 510(k) K961578

Name: FDA 510(k) clearance K961578
Creator: U.S. Food and Drug Administration
Published: 1996-07-10

Substantially Equivalent

United States Surgical, A Division of Tyco Healthc

FDA 510(k) clearance K961578 for SUTURE ANCHOR, Substantially Equivalent on 1996-07-10. Applicant: United States Surgical, A Division of Tyco Healthc. Device class: 2.

Clearance details

Applicant: United States Surgical, A Division of Tyco Healthc
Product code: Code JDR
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 1996-04-24
Decision date: 1996-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

Download summary PDF View on FDA.gov ↗

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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.