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FDA 510(k)

Anovo Pedestal

K-Number: K232146 · 2023-09-14

Decision Date2023-09-14
Product CodeQNM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Anovo Pedestal is a medical device manufactured by Momentis Surgical , Ltd.. It received FDA 510(k) clearance on 2023-09-14 under approval number K232146. The device is classified under product code QNM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Anovo Pedestal?

Anovo Pedestal is a medical device that received FDA 510(k) clearance on 2023-09-14. It is manufactured by Momentis Surgical , Ltd.. The 510(k) number is K232146.

When was Anovo Pedestal approved by the FDA?

Anovo Pedestal received FDA 510(k) clearance on 2023-09-14, under approval number K232146.

What company makes Anovo Pedestal?

Anovo Pedestal is manufactured by Momentis Surgical , Ltd..

What is the FDA product code for Anovo Pedestal?

The FDA product code for Anovo Pedestal is QNM.

Other Devices by Momentis Surgical , Ltd.

View all 8 devices →

Related Devices (Code: QNM)

Official Source

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