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MAKOPLASTY TOTAL HIP ALLPICATION, RIO STANDARD SYSTEM

K141989 Class II Special
Decision Date
2014-11-13
Sponsor / Applicant
Mako Surgical Corporation

Technical Specification

510(k) Submission ID K141989
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2014-11-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAKOPLASTY TOTAL HIP ALLPICATION, RIO STANDARD SYSTEM received FDA 510(k) clearance under submission number K141989, sponsored by Mako Surgical Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2014-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.