Varioguide Drill Kit
FDA 510(k) K132436 · Mri Interventions, Inc.
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
Other 510(k)s with product code HBE
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253627 | Surgify Halo (54.085.SHD.U1); Surgify Halo (54.140.SHD. U1); Surgify Halo…HBE · Traditional | Surgify Medical OY | 03/26/2026SE |
| K250815 | Hubly Drill (H100)HBE · Traditional | Hubly, Inc. | 11/06/2025SE |
| K252060 | GreenHBE · Traditional | Phasor Health, LLC | 10/31/2025SE |
| K252662 | UniBurHBE · Traditional | Nakanishi, Inc. | 09/19/2025SE |
| K251433 | Surgify Halo (54.085.SHD.H1); Surgify Halo (54.140.SHD.H1); Surgify Halo…HBE · Special | Surgify Medical OY | 06/04/2025SE |
| K250380 | Surgify Halo (54.085.SHD.H1); Surgify Halo (54.140.SHD.H1); Surgify Halo…HBE · Special | Surgify Medical OY | 03/13/2025SE |
| K250374 | iBur 3.0mm Diamond Match Head, Distal Bend (8431-107-030D); iBur 3.0mm Precision Round…HBE · Special | Stryker Instruments | 03/11/2025SE |
| K232684 | Surgify HaloHBE · Traditional | Surgify Medical OY | 11/29/2023SE |
| K230619 | Hubly Electric Drill (H100)HBE · Traditional | Hubly, Inc. | 05/04/2023SE |
| K223199 | 2.1 x 255mm Drill, 22mm StopHBE · Special | Biomet Microfixation | 11/15/2022SE |
More from Biomet Microfixation
| 510(k) | Device | Decision |
|---|---|---|
| K200079 | ClearPoint System and AccessoriesHAW · Special | 02/13/2020SE |
| K191701 | Arcus Head Fixation FrameHBL · Traditional | 11/15/2019SE |
| K191400 | Voyager Trajectory Array Guide (V-TAG)HAW · Special | 06/21/2019SE |
| K181731 | MR Compatible Aspiration KitGWG · Traditional | 11/20/2018SE |
| K181195 | ClearPoint SystemORR · Traditional | 11/02/2018SE |
| K171257 | ClearPoint SystemORR · Traditional | 10/20/2017SE |
| K160129 | MRII Cranial Drill and AccessoriesHBG · Special | 03/26/2016SE |
| K160434 | ClearPoint SystemHAW · Special | 03/17/2016SE |
| K142505 | ClearPoint SystemHAW · Traditional | 10/21/2015SE |
| K151536 | SmartTwist MRII Hand Drill, SmartTip MRII Drill bit Kit, 4.5mm, 6.0mmHBG · Special | 07/08/2015SE |
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.