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HIP FRACTURE STEM SYSTEM

K883179 Class II Traditional
Decision Date
1988-09-22
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K883179
Product Code KWL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1988-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIP FRACTURE STEM SYSTEM received FDA 510(k) clearance under submission number K883179, 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 1988-09-22.

Classification & Regulation

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