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MODIFICATION TO: QUANTUM VERTEBRAL BODY REPLACEMENT

K052641 Class II Special
Decision Date
2006-04-12
Sponsor / Applicant
Quantum Orthopedics, Inc.

Technical Specification

510(k) Submission ID K052641
Product Code MQP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2006-04-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: QUANTUM VERTEBRAL BODY REPLACEMENT received FDA 510(k) clearance under submission number K052641, sponsored by Quantum Orthopedics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-04-12.

Classification & Regulation

This clearance is catalogued under FDA product code MQP and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.