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FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE REP

K853730 Class II Traditional
Decision Date
1986-02-18
Sponsor / Applicant
Protek, Inc.

Technical Specification

510(k) Submission ID K853730
Product Code MBV
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 1986-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE REP received FDA 510(k) clearance under submission number K853730, sponsored by Protek, 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 1986-02-18.

Classification & Regulation

This clearance is catalogued under FDA product code MBV and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.