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SUSPENSION CLAVICLE FRACTURE FIXATION SYSTEM

K102095 Class II Traditional
Decision Date
2010-12-07
Sponsor / Applicant
Suspension Orthopaedic Solutions, LLC

Technical Specification

510(k) Submission ID K102095
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2010-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUSPENSION CLAVICLE FRACTURE FIXATION SYSTEM received FDA 510(k) clearance under submission number K102095, sponsored by Suspension Orthopaedic Solutions, 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 2010-12-07.

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.