meddevicedb.com FDA Device Reference

DB-Orthopedics

K200752 Class II Traditional
Decision Date
2020-04-22
Sponsor / Applicant
Dimensional Bioceramics, LLC

Technical Specification

510(k) Submission ID K200752
Product Code MQV
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3045
Decision Date 2020-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DB-Orthopedics received FDA 510(k) clearance under submission number K200752, sponsored by Dimensional Bioceramics, 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 2020-04-22.

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.