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FDA 510(k)

Symani Surgical System (820-03830)

K-Number: K250014 · 2025-01-27

Decision Date2025-01-27
Product CodeSAQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Symani Surgical System (820-03830) is a medical device manufactured by Medical Microinstruments, Inc.. It received FDA 510(k) clearance on 2025-01-27 under approval number K250014. The device is classified under product code SAQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Symani Surgical System (820-03830)?

Symani Surgical System (820-03830) is a medical device that received FDA 510(k) clearance on 2025-01-27. It is manufactured by Medical Microinstruments, Inc.. The 510(k) number is K250014.

When was Symani Surgical System (820-03830) approved by the FDA?

Symani Surgical System (820-03830) received FDA 510(k) clearance on 2025-01-27, under approval number K250014.

What company makes Symani Surgical System (820-03830)?

Symani Surgical System (820-03830) is manufactured by Medical Microinstruments, Inc..

What is the FDA product code for Symani Surgical System (820-03830)?

The FDA product code for Symani Surgical System (820-03830) is SAQ.

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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.