meddevicedb.com FDA Device Reference

Uni-FuZe-C Bone Strip

K221726 Class II Traditional
Decision Date
2023-01-18
Sponsor / Applicant
Zavation Medical Products, LLC

Technical Specification

510(k) Submission ID K221726
Product Code MQV
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3045
Decision Date 2023-01-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Uni-FuZe-C Bone Strip received FDA 510(k) clearance under submission number K221726, sponsored by Zavation Medical Products, 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 2023-01-18.

Classification & Regulation

This clearance is catalogued under FDA product code MQV and 21 CFR 888.3045, within the Orthopedic review panel as a Class II device.