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FDA 510(k)

DSG Connect Technology

K-Number: K201454 · 2021-02-10

ApplicantSpineguard S.A.
Decision Date2021-02-10
Product CodePDQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DSG Connect Technology is a medical device manufactured by Spineguard S.A.. It received FDA 510(k) clearance on 2021-02-10 under approval number K201454. The device is classified under product code PDQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSG Connect Technology?

DSG Connect Technology is a medical device that received FDA 510(k) clearance on 2021-02-10. It is manufactured by Spineguard S.A.. The 510(k) number is K201454.

When was DSG Connect Technology approved by the FDA?

DSG Connect Technology received FDA 510(k) clearance on 2021-02-10, under approval number K201454.

What company makes DSG Connect Technology?

DSG Connect Technology is manufactured by Spineguard S.A..

What is the FDA product code for DSG Connect Technology?

The FDA product code for DSG Connect Technology is PDQ.

Related Clinical Trials

NCT06714097 Application of Digital Twins' Technology in Patients Who Had a Stroke, With Moyamoya Disease and With Cerebral Amyloid Angiopathy (CAA) During the Secondary Prevention Phase: A Proof of Concept Using a Randomized Control Trial (Clinical Study 6, STRATIF-AI Project) RECRUITING

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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