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FDA 510(k)

Modular Toga

K-Number: K200977 · 2020-08-05

ApplicantOperating Room Innovations, Inc.
Decision Date2020-08-05
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Modular Toga is a medical device manufactured by Operating Room Innovations, Inc.. It received FDA 510(k) clearance on 2020-08-05 under approval number K200977. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Modular Toga?

Modular Toga is a medical device that received FDA 510(k) clearance on 2020-08-05. It is manufactured by Operating Room Innovations, Inc.. The 510(k) number is K200977.

When was Modular Toga approved by the FDA?

Modular Toga received FDA 510(k) clearance on 2020-08-05, under approval number K200977.

What company makes Modular Toga?

Modular Toga is manufactured by Operating Room Innovations, Inc..

What is the FDA product code for Modular Toga?

The FDA product code for Modular Toga is FYA.

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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.

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