meddevicedb.com FDA Device Reference

BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS

K032700 Class II Special
Decision Date
2003-10-09
Sponsor / Applicant
Blackstone Medical, Inc.

Technical Specification

510(k) Submission ID K032700
Product Code MQP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2003-10-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS received FDA 510(k) clearance under submission number K032700, sponsored by Blackstone Medical, 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 2003-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code MQP and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.