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VHS PEDIATRIC HIP SCREW SYSTEM

K011603 Class II Traditional
Decision Date
2001-08-15
Sponsor / Applicant
Walter Abendschein, M.D.

Technical Specification

510(k) Submission ID K011603
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2001-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VHS PEDIATRIC HIP SCREW SYSTEM received FDA 510(k) clearance under submission number K011603, sponsored by Walter Abendschein, M.D.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-08-15.

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.