meddevicedb.com FDA Device Reference

Renovo Life Hard Carbon Coated Drill Bit

K151661 Class I Traditional
Decision Date
2016-01-15
Sponsor / Applicant
Renovo Life, LLC

Technical Specification

510(k) Submission ID K151661
Product Code HTW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4540
Decision Date 2016-01-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Renovo Life Hard Carbon Coated Drill Bit received FDA 510(k) clearance under submission number K151661, sponsored by Renovo Life, 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 2016-01-15.

Classification & Regulation

This clearance is catalogued under FDA product code HTW and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.