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WUJIN #3 TIBIAL NAIL

K002325 Class II Traditional
Decision Date
2000-10-30
Sponsor / Applicant
Biologically Oriented Prostheses

Technical Specification

510(k) Submission ID K002325
Product Code JDS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2000-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WUJIN #3 TIBIAL NAIL received FDA 510(k) clearance under submission number K002325, sponsored by Biologically Oriented Prostheses. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code JDS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.