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RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS

K112897 Class II Traditional
Decision Date
2012-06-13
Sponsor / Applicant
Renovis Surgical Technologies, LLC

Technical Specification

510(k) Submission ID K112897
Product Code OQG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2012-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS received FDA 510(k) clearance under submission number K112897, sponsored by Renovis Surgical Technologies, 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 2012-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code OQG and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.