Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Maestro System (REF100)

K-Number: K240598 · 2024-06-03

ApplicantMoon Surgical
Decision Date2024-06-03
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Maestro System (REF100) is a medical device manufactured by Moon Surgical. It received FDA 510(k) clearance on 2024-06-03 under approval number K240598. 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 System (REF100)?

Maestro System (REF100) is a medical device that received FDA 510(k) clearance on 2024-06-03. It is manufactured by Moon Surgical. The 510(k) number is K240598.

When was Maestro System (REF100) approved by the FDA?

Maestro System (REF100) received FDA 510(k) clearance on 2024-06-03, under approval number K240598.

What company makes Maestro System (REF100)?

Maestro System (REF100) is manufactured by Moon Surgical.

What is the FDA product code for Maestro System (REF100)?

The FDA product code for Maestro System (REF100) is FQO.

Other Devices by Moon Surgical

K221410Maestro Platform K250984Maestro System (REF100) K242323Maestro System (REF100)

Related Devices (Code: FQO)

K221410Maestro PlatformMoon Surgical

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.

↑