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SUMMIT SI OCT Spinal Fixation System, MOUNTAINEER OCT Spinal System

K151885 Class II Traditional
Decision Date
2015-09-03
Sponsor / Applicant
Depuy Synthes, Inc.

Technical Specification

510(k) Submission ID K151885
Product Code NKG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3075
Decision Date 2015-09-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUMMIT SI OCT Spinal Fixation System, MOUNTAINEER OCT Spinal System received FDA 510(k) clearance under submission number K151885, sponsored by Depuy Synthes, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-09-03.

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.