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UTF STEM-REDUCED, ADDITIONAL SIZES

K132207 Class II Special
Decision Date
2013-08-30
Sponsor / Applicant
United Orthopedic Corporation

Technical Specification

510(k) Submission ID K132207
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2013-08-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UTF STEM-REDUCED, ADDITIONAL SIZES received FDA 510(k) clearance under submission number K132207, sponsored by United Orthopedic Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-08-30.

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.