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 a medical device manufactured by Artaflex, Inc.. It received FDA 510(k) clearance on 2024-02-08 under approval 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. It is manufactured by Artaflex, Inc.. The 510(k) number is K231575.
When was Vecttor VT-300 approved by the FDA?
Vecttor VT-300 received FDA 510(k) clearance on 2024-02-08, under approval number K231575.
What company makes Vecttor VT-300?
Vecttor VT-300 is manufactured by Artaflex, Inc..
What is the FDA product code for Vecttor VT-300?
The FDA product code for Vecttor VT-300 is LIH.
Related Devices (Code: LIH)
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.