DSG Connect Technology
FDA 510(k) K201454 · Spineguard S.A.
510(k) numberK201454
Submission
- Device name
- DSG Connect Technology
- Applicant
- Spineguard S.A.
Vincennes, FR - Received
- June 1, 2020
- Decision date
- February 10, 2021
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- PDQ – Neurosurgical Nerve Locator
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.1820
- Specialty
- Ear, Nose, Throat
To locate or monitor function of spinal nerve roots or peripheral nerves during neurosurgery.
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| K243636 | Neuralytix iD3 System (NTX-9001)PDQ · Traditional | Neuralytix, LLC | 06/26/2025SE |
| K223438 | TELIGEN System Peripheral Motor Nerve Stimulation IndicationsPDQ · Traditional | Medos International SARL | 02/10/2023SE |
| K221821 | ATEC IOM Accessory InstrumentsPDQ · Traditional | Alphatec Spine, Inc. | 09/23/2022SE |
| K220160 | PediGuard ThreadedPDQ · Traditional | Spineguard S.A. | 03/31/2022SE |
| K203684 | Neurosign V4 Intraoperative Nerve MonitorPDQ · Traditional | Magstim Company, Ltd. | 03/17/2021SE |
| K191723 | ATEC IOM Accessory InstrumentsPDQ · Traditional | Alphatec Spine, Inc. | 10/18/2019SE |
| K190163 | ALARA Neuro Access KitPDQ · Traditional | SurGenTec, LLC | 07/16/2019SE |
| K182617 | ATEC IOM Accessory InstrumentsPDQ · Traditional | Alphatec Spine, Inc. | 05/09/2019SE |
More from Alphatec Spine, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K220160 | PediGuard ThreadedPDQ · Traditional | 03/31/2022SE |
| K162884 | SpineGuard DSG Zavation Screw SystemHBG · Traditional | 01/12/2017SE |
| K152747 | DSG Threaded Drill SystemPDQ · Traditional | 06/10/2016SE |
| K143159 | Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2, Cannulated PediGuard…PDQ · Traditional | 01/23/2015SE |
| K123390 | Pediguard Nerve Detector SystemPDQ · Traditional | 08/08/2013SE |
Questions and answers
When was DSG Connect Technology cleared by the FDA?
DSG Connect Technology (K201454) received a 510(k) decision of Substantially Equivalent on February 10, 2021, 254 days after the submission was received.
What is the product code of K201454?
The FDA product code is PDQ – Neurosurgical Nerve Locator, a Class II (moderate risk) device regulated under 21 CFR 874.1820.