meddevicedb.com FDA Device Reference

Ascendant TM Cervical Spacer System

K150130 Class II Traditional
Decision Date
2015-05-28
Sponsor / Applicant
Exactech, Inc.

Technical Specification

510(k) Submission ID K150130
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2015-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ascendant TM Cervical Spacer System received FDA 510(k) clearance under submission number K150130, sponsored by Exactech, 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 2015-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code ODP and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.