meddevicedb.com FDA Device Reference

FORTEZZA Spinal Stabilization System

K162576 Class II Traditional
Decision Date
2016-11-10
Sponsor / Applicant
Osso Surgical

Technical Specification

510(k) Submission ID K162576
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2016-11-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FORTEZZA Spinal Stabilization System received FDA 510(k) clearance under submission number K162576, sponsored by Osso Surgical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-11-10.

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.