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FINGER JOINT PROSTHESIS

K013629 Class II Traditional
Decision Date
2002-01-25
Sponsor / Applicant
Avanta Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K013629
Product Code KYJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3230
Decision Date 2002-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FINGER JOINT PROSTHESIS received FDA 510(k) clearance under submission number K013629, sponsored by Avanta Orthopaedics, 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 2002-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code KYJ and 21 CFR 888.3230, within the Orthopedic review panel as a Class II device.