FDA 510(k)

Maestro Platform

K-Number: K221410 · 2022-12-02

Decision Date2022-12-02

Product CodeFQO

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Maestro Platform is the device name listed in this FDA 510(k) record. The listed applicant is Moon Surgical. It received FDA 510(k) clearance on 2022-12-02 under 510(k) 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. The listed applicant is Moon Surgical. The 510(k) number is K221410.

When did Maestro Platform receive FDA 510(k) clearance?

Maestro Platform received FDA 510(k) clearance on 2022-12-02, under 510(k) number K221410.

Who is the listed applicant for Maestro Platform?

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

What is the FDA product code for Maestro Platform?

The FDA product code for Maestro Platform is FQO.

Other records listing Moon Surgical 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.

K250984Maestro System (REF100)K242323Maestro System (REF100)K240598Maestro System (REF100)

Related Devices (Code: FQO)

K240598Maestro System (REF100)Moon Surgical

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.