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DOUBLE BALL JOINT

K803166 Class II Traditional
Decision Date
1981-01-09
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K803166
Product Code JEC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 1981-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOUBLE BALL JOINT received FDA 510(k) clearance under submission number K803166, 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 1981-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code JEC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.