meddevicedb.com FDA Device Reference

AUFRANC-TURNER ATS TOTAL HIP SYSTEM

K802872 Class II Traditional
Decision Date
1980-12-11
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K802872
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1980-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUFRANC-TURNER ATS TOTAL HIP SYSTEM received FDA 510(k) clearance under submission number K802872, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1980-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.