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BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER

K040034 Class II Special
Decision Date
2004-02-11
Sponsor / Applicant
Blackstone Medical, Inc.

Technical Specification

510(k) Submission ID K040034
Product Code MNI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2004-02-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER received FDA 510(k) clearance under submission number K040034, 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 2004-02-11.

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.