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FDA 510(k)

VitruvianScan (v1.0)

K-Number: K241925 · 2024-10-02

ApplicantPerspectum, Ltd.
Decision Date2024-10-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VitruvianScan (v1.0) is a medical device manufactured by Perspectum, Ltd.. It received FDA 510(k) clearance on 2024-10-02 under approval number K241925. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VitruvianScan (v1.0)?

VitruvianScan (v1.0) is a medical device that received FDA 510(k) clearance on 2024-10-02. It is manufactured by Perspectum, Ltd.. The 510(k) number is K241925.

When was VitruvianScan (v1.0) approved by the FDA?

VitruvianScan (v1.0) received FDA 510(k) clearance on 2024-10-02, under approval number K241925.

What company makes VitruvianScan (v1.0)?

VitruvianScan (v1.0) is manufactured by Perspectum, Ltd..

What is the FDA product code for VitruvianScan (v1.0)?

The FDA product code for VitruvianScan (v1.0) is LNH.

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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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