K-WIRE— 510(k) K903264

Substantially Equivalent

Onyx Medical Corp.

FDA 510(k) clearance K903264 for K-WIRE, Substantially Equivalent on 1990-07-30. Applicant: Onyx Medical Corp..

Clearance details

Applicant: Onyx Medical Corp.
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 1990-07-24
Decision date: 1990-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.