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TAYLOR SPATIAL FRAME EXTERNAL FIXATION SYSTEM

K970748 Class II Traditional
Decision Date
1997-05-09
Sponsor / Applicant
Smith & Nephew, Inc., Orthopaedic Div.

Technical Specification

510(k) Submission ID K970748
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1997-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAYLOR SPATIAL FRAME EXTERNAL FIXATION SYSTEM received FDA 510(k) clearance under submission number K970748, sponsored by Smith & Nephew, Inc., Orthopaedic Div.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1997-05-09.

Classification & Regulation

This clearance is catalogued under FDA product code KTT and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.