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MIDAS REX MR7 PNEUMATIC HIGH SPEED SYSTEM, MODELS PM700, PM710, PC700, PC710, PC720, PA700

K090112 Class II Traditional
Decision Date
2009-03-26
Sponsor / Applicant
Medtronic Powered Surgical Solutions

Technical Specification

510(k) Submission ID K090112
Product Code HBB
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4370
Decision Date 2009-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MIDAS REX MR7 PNEUMATIC HIGH SPEED SYSTEM, MODELS PM700, PM710, PC700, PC710, PC720, PA700 received FDA 510(k) clearance under submission number K090112, sponsored by Medtronic Powered Surgical Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2009-03-26.

Classification & Regulation

This clearance is catalogued under FDA product code HBB and 21 CFR 882.4370, within the Neurology review panel as a Class II device.