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FDA 510(k)

Vecttor VT-300

K-Number: K231575 · 2024-02-08

ApplicantArtaflex, Inc.
Decision Date2024-02-08
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Vecttor VT-300 is the device name listed in this FDA 510(k) record. The listed applicant is Artaflex, Inc.. It received FDA 510(k) clearance on 2024-02-08 under 510(k) number K231575. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vecttor VT-300?

Vecttor VT-300 is a medical device that received FDA 510(k) clearance on 2024-02-08. The listed applicant is Artaflex, Inc.. The 510(k) number is K231575.

When did Vecttor VT-300 receive FDA 510(k) clearance?

Vecttor VT-300 received FDA 510(k) clearance on 2024-02-08, under 510(k) number K231575.

Who is the listed applicant for Vecttor VT-300?

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

What is the FDA product code for Vecttor VT-300?

The FDA product code for Vecttor VT-300 is LIH.

Related Devices (Code: LIH)

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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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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