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G Surgical OCT Spinal System

K171834 Class II Traditional
Decision Date
2017-12-19
Sponsor / Applicant
G Surgical, LLC

Technical Specification

510(k) Submission ID K171834
Product Code NKG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3075
Decision Date 2017-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

G Surgical OCT Spinal System received FDA 510(k) clearance under submission number K171834, sponsored by G Surgical, 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 2017-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code NKG and 21 CFR 888.3075, within the Orthopedic review panel as a Class II device.