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QUANTUM SPINAL SYSTEM

K070973 Class II Traditional
Decision Date
2007-07-03
Sponsor / Applicant
Pioneer Surgical Technology

Technical Specification

510(k) Submission ID K070973
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2007-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTUM SPINAL SYSTEM received FDA 510(k) clearance under submission number K070973, sponsored by Pioneer Surgical Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-07-03.

Classification & Regulation

This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.