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HOWMEDICA STRAIGHT STEM FEMORAL COMPONENT

K940307 Class II Traditional
Decision Date
1995-01-19
Sponsor / Applicant
Howmedica, Inc.

Technical Specification

510(k) Submission ID K940307
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1995-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOWMEDICA STRAIGHT STEM FEMORAL COMPONENT received FDA 510(k) clearance under submission number K940307, sponsored by Howmedica, 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 1995-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.