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EBI X FIX DYNAFIX MINI EXTERNAL FIXATION SYSTEM

K970290 Class II Traditional
Decision Date
1997-04-01
Sponsor / Applicant
Ebi, L.P.

Technical Specification

510(k) Submission ID K970290
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1997-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EBI X FIX DYNAFIX MINI EXTERNAL FIXATION SYSTEM received FDA 510(k) clearance under submission number K970290, sponsored by Ebi, L.P.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1997-04-01.

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.