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PASS SPINAL SYSTEM

K013431 Class II Special
Decision Date
2001-11-15
Sponsor / Applicant
Encore Orthopedics, Inc.

Technical Specification

510(k) Submission ID K013431
Product Code MNI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2001-11-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PASS SPINAL SYSTEM received FDA 510(k) clearance under submission number K013431, sponsored by Encore Orthopedics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-11-15.

Classification & Regulation

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