meddevicedb.com FDA Device Reference

SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM

K072116 Class II Traditional
Decision Date
2008-03-20
Sponsor / Applicant
Neurospine Innovations and Solutions

Technical Specification

510(k) Submission ID K072116
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2008-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM received FDA 510(k) clearance under submission number K072116, sponsored by Neurospine Innovations and Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-03-20.

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.