meddevicedb.com FDA Device Reference

PASS LP SPINAL SYSTEM

K110497 Class II Special
Decision Date
2011-09-26
Sponsor / Applicant
Medicrea International

Technical Specification

510(k) Submission ID K110497
Product Code MNH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2011-09-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PASS LP SPINAL SYSTEM received FDA 510(k) clearance under submission number K110497, sponsored by Medicrea International. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-09-26.

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.