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ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM

K990481 Class II Traditional
Decision Date
1999-03-17
Sponsor / Applicant
Biodynamic Technologies, Inc.

Technical Specification

510(k) Submission ID K990481
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1999-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM received FDA 510(k) clearance under submission number K990481, sponsored by Biodynamic Technologies, 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 1999-03-17.

Classification & Regulation

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