CANNULATED PLUS HIP SCREW— 510(k) K952640

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K952640 for CANNULATED PLUS HIP SCREW, Substantially Equivalent on 1995-07-31. Applicant: Wrightmedicaltechnologyinc.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code JDW
Advisory panel: Orthopedic
Date received: 1995-06-09
Decision date: 1995-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code JDW

product code JDW

Injury: 717
Total: 717

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.