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HIP PROSTHESIS -VARIOUS

K831420 Class II Traditional
Decision Date
1983-09-20
Sponsor / Applicant
The Oec Group

Technical Specification

510(k) Submission ID K831420
Product Code KWL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1983-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIP PROSTHESIS -VARIOUS received FDA 510(k) clearance under submission number K831420, sponsored by The Oec Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1983-09-20.

Classification & Regulation

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