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FDA 510(k)

Anovo Surgical System (Model 6Ne)

K-Number: K242157 · 2024-10-21

Decision Date2024-10-21
Product CodeQNM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Anovo Surgical System (Model 6Ne) 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 2024-10-21 under 510(k) number K242157. 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 Surgical System (Model 6Ne)?

Anovo Surgical System (Model 6Ne) is a medical device that received FDA 510(k) clearance on 2024-10-21. The listed applicant is Momentis Surgical , Ltd.. The 510(k) number is K242157.

When did Anovo Surgical System (Model 6Ne) receive FDA 510(k) clearance?

Anovo Surgical System (Model 6Ne) received FDA 510(k) clearance on 2024-10-21, under 510(k) number K242157.

Who is the listed applicant for Anovo Surgical System (Model 6Ne)?

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 Surgical System (Model 6Ne)?

The FDA product code for Anovo Surgical System (Model 6Ne) 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

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