Maestro Platform
K-Number: K221410 · 2022-12-02
ApplicantMoon Surgical
Decision Date2022-12-02
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Maestro Platform is a medical device manufactured by Moon Surgical. It received FDA 510(k) clearance on 2022-12-02 under approval number K221410. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Maestro Platform?
Maestro Platform is a medical device that received FDA 510(k) clearance on 2022-12-02. It is manufactured by Moon Surgical. The 510(k) number is K221410.
When was Maestro Platform approved by the FDA?
Maestro Platform received FDA 510(k) clearance on 2022-12-02, under approval number K221410.
What company makes Maestro Platform?
Maestro Platform is manufactured by Moon Surgical.
What is the FDA product code for Maestro Platform?
The FDA product code for Maestro Platform is FQO.
Other Devices by Moon Surgical
Related Devices (Code: FQO)
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.