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WEBER-STUHMER HIP PROSTHESIS STEM

K841391 Class II Traditional
Decision Date
1984-04-13
Sponsor / Applicant
Allo Pro Corp.

Technical Specification

510(k) Submission ID K841391
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1984-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WEBER-STUHMER HIP PROSTHESIS STEM received FDA 510(k) clearance under submission number K841391, sponsored by Allo Pro 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 1984-04-13.

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.