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PICCOLO COMPOSITE ANKLE ARTHRODESIS NAILING SYSTEM

K123810 Class II Traditional
Decision Date
2013-06-14
Sponsor / Applicant
CarboFix Orthopedics , Ltd.

Technical Specification

510(k) Submission ID K123810
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2013-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PICCOLO COMPOSITE ANKLE ARTHRODESIS NAILING SYSTEM received FDA 510(k) clearance under submission number K123810, sponsored by CarboFix Orthopedics , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.