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STABILIZ FIXATION SYSTEM - SPL LOCKING SCREW

K130731 Class II Traditional
Decision Date
2013-07-19
Sponsor / Applicant
Stabiliz Orthopaedics, LLC

Technical Specification

510(k) Submission ID K130731
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2013-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STABILIZ FIXATION SYSTEM - SPL LOCKING SCREW received FDA 510(k) clearance under submission number K130731, sponsored by Stabiliz Orthopaedics, 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 2013-07-19.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.