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DUAL TAPER WEDGE PRESSED FIT FEMORAL COMPONENT

K953268 Class II Traditional
Decision Date
1996-01-17
Sponsor / Applicant
Stelkast Company

Technical Specification

510(k) Submission ID K953268
Product Code LWJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1996-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUAL TAPER WEDGE PRESSED FIT FEMORAL COMPONENT received FDA 510(k) clearance under submission number K953268, sponsored by Stelkast Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1996-01-17.

Classification & Regulation

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