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MotoBAND CP Implant System

K173710 Class II Special
Decision Date
2018-02-12
Sponsor / Applicant
Crossroads Extremity Systems, LLC

Technical Specification

510(k) Submission ID K173710
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2018-02-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MotoBAND CP Implant System received FDA 510(k) clearance under submission number K173710, sponsored by Crossroads Extremity Systems, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2018-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.