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ANITOMIC TOTAL HIP SYSTEM

K800050 Class II Traditional
Decision Date
1980-01-24
Sponsor / Applicant
Hexcel Medical

Technical Specification

510(k) Submission ID K800050
Product Code JDG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1980-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANITOMIC TOTAL HIP SYSTEM received FDA 510(k) clearance under submission number K800050, sponsored by Hexcel Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1980-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code JDG and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.