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EXTREMITY MEDICAL TRAPEZIUM PROSTHESIS

K092548 Class II Traditional
Decision Date
2009-12-15
Sponsor / Applicant
Extremity Medical, LLC

Technical Specification

510(k) Submission ID K092548
Product Code KYI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3770
Decision Date 2009-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTREMITY MEDICAL TRAPEZIUM PROSTHESIS received FDA 510(k) clearance under submission number K092548, sponsored by Extremity Medical, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-12-15.

Classification & Regulation

This clearance is catalogued under FDA product code KYI and 21 CFR 888.3770, within the Orthopedic review panel as a Class II device.