Varioguide Drill Kit

FDA 510(k) K132436 · Mri Interventions, Inc.

Substantially Equivalent

510(k) numberK132436

Submission

Device name
Varioguide Drill Kit
Applicant
Mri Interventions, Inc.
Irvine, CA, US
Received
August 5, 2013
Decision date
March 20, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HBE – Drills, Burrs, Trephines & Accessories (Simple, Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 882.4310
Specialty
Neurology

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K252060GreenHBE · Traditional Phasor Health, LLC10/31/2025SE
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K251433Surgify Halo (54.085.SHD.H1); Surgify Halo (54.140.SHD.H1); Surgify Halo…HBE · Special Surgify Medical OY06/04/2025SE
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K232684Surgify HaloHBE · Traditional Surgify Medical OY11/29/2023SE
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K2231992.1 x 255mm Drill, 22mm StopHBE · Special Biomet Microfixation11/15/2022SE

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Questions and answers

When was Varioguide Drill Kit cleared by the FDA?

Varioguide Drill Kit (K132436) received a 510(k) decision of Substantially Equivalent on March 20, 2014, 227 days after the submission was received.

What is the product code of K132436?

The FDA product code is HBE – Drills, Burrs, Trephines & Accessories (Simple, Powered), a Class II (moderate risk) device regulated under 21 CFR 882.4310.