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THE SELBY SYSTEM

K920102 Class II Traditional
Decision Date
1992-05-05
Sponsor / Applicant
Advanced Spine Fixation Systems, Inc.

Technical Specification

510(k) Submission ID K920102
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 1992-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE SELBY SYSTEM received FDA 510(k) clearance under submission number K920102, sponsored by Advanced Spine Fixation Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1992-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code KWP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.