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KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALL

K920219 Class II Traditional
Decision Date
1992-10-30
Sponsor / Applicant
Kinamed, Inc.

Technical Specification

510(k) Submission ID K920219
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 1992-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALL received FDA 510(k) clearance under submission number K920219, sponsored by Kinamed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1992-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.