FDA 510(k)

V-Print splint

K-Number: K201091 · 2020-11-06

Decision Date2020-11-06

Product CodeMQC

DecisionSubstantially Equivalent

Device Summary

V-Print splint is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2020-11-06 under 510(k) number K201091. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-Print splint?

V-Print splint is a medical device that received FDA 510(k) clearance on 2020-11-06. The listed applicant is Voco GmbH. The 510(k) number is K201091.

When did V-Print splint receive FDA 510(k) clearance?

V-Print splint received FDA 510(k) clearance on 2020-11-06, under 510(k) number K201091.

Who is the listed applicant for V-Print splint?

The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-Print splint?

The FDA product code for V-Print splint is MQC.

Other records listing Voco GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MQC)

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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.