Anovo Surgical System (model 6N)
K-Number: K241907 · 2024-10-02
Device Summary
Frequently Asked Questions
What is the Anovo Surgical System (model 6N)?
Anovo Surgical System (model 6N) is a medical device that received FDA 510(k) clearance on 2024-10-02. The listed applicant is Momentis Surgical , Ltd.. The 510(k) number is K241907.
When did Anovo Surgical System (model 6N) receive FDA 510(k) clearance?
Anovo Surgical System (model 6N) received FDA 510(k) clearance on 2024-10-02, under 510(k) number K241907.
Who is the listed applicant for Anovo Surgical System (model 6N)?
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 6N)?
The FDA product code for Anovo Surgical System (model 6N) 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.
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.