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SCS CLOSED SCREW

K003733 Class II Traditional
Decision Date
2001-05-29
Sponsor / Applicant
Ortho Tec, LLC

Technical Specification

510(k) Submission ID K003733
Product Code MNH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2001-05-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCS CLOSED SCREW received FDA 510(k) clearance under submission number K003733, sponsored by Ortho Tec, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-05-29.

Classification & Regulation

This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.