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PRECISION HIP LONG STEM FEMORAL COMPONENT SYSTEM

K873089 Class II Traditional
Decision Date
1987-09-16
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K873089
Product Code JDG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1987-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRECISION HIP LONG STEM FEMORAL COMPONENT SYSTEM received FDA 510(k) clearance under submission number K873089, 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 1987-09-16.

Classification & Regulation

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