meddevicedb.com FDA Device Reference

EBI XFIX VISION FIXATION SYSTEM

K993886 Class II Special
Decision Date
1999-12-14
Sponsor / Applicant
Ebi, L.P.

Technical Specification

510(k) Submission ID K993886
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1999-12-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EBI XFIX VISION FIXATION SYSTEM received FDA 510(k) clearance under submission number K993886, sponsored by Ebi, L.P.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-12-14.

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.