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PROPHECY INFINITY PREOPERATIVE NAVIGATION ALIGNMENT GUIDES

K131283 Class II Traditional
Decision Date
2013-07-05
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K131283
Product Code HSN
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3110
Decision Date 2013-07-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROPHECY INFINITY PREOPERATIVE NAVIGATION ALIGNMENT GUIDES received FDA 510(k) clearance under submission number K131283, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-07-05.

Classification & Regulation

This clearance is catalogued under FDA product code HSN and 21 CFR 888.3110, within the Orthopedic review panel as a Class II device.