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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 the device name listed in this FDA 510(k) record. The listed applicant is Momentis Surgical , Ltd.. It received FDA 510(k) clearance on 2023-09-14 under 510(k) 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. The listed applicant is Momentis Surgical , Ltd.. The 510(k) number is K232146.

When did Anovo Pedestal receive FDA 510(k) clearance?

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

Who is the listed applicant for Anovo Pedestal?

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

What is the FDA product code for Anovo Pedestal?

The FDA product code for Anovo Pedestal is QNM.

Other records listing Momentis Surgical , Ltd. 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.

View all 8 devices →

Related Devices (Code: QNM)

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.

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.