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ICONACY(TM) I-Hip(TM)

K160266 Class II Special
Decision Date
2016-04-08
Sponsor / Applicant
Iconacy Orthopedic Implants, LLC

Technical Specification

510(k) Submission ID K160266
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2016-04-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ICONACY(TM) I-Hip(TM) received FDA 510(k) clearance under submission number K160266, sponsored by Iconacy Orthopedic Implants, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-04-08.

Classification & Regulation

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