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FDA 510(k)

Responsive Arthroscopy Thunderbolt System

K-Number: K203121 · 2021-04-27

ApplicantResponsive Arthroscopy, LLC
Decision Date2021-04-27
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Responsive Arthroscopy Thunderbolt System is a medical device manufactured by Responsive Arthroscopy, LLC. It received FDA 510(k) clearance on 2021-04-27 under approval number K203121. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Responsive Arthroscopy Thunderbolt System?

Responsive Arthroscopy Thunderbolt System is a medical device that received FDA 510(k) clearance on 2021-04-27. It is manufactured by Responsive Arthroscopy, LLC. The 510(k) number is K203121.

When was Responsive Arthroscopy Thunderbolt System approved by the FDA?

Responsive Arthroscopy Thunderbolt System received FDA 510(k) clearance on 2021-04-27, under approval number K203121.

What company makes Responsive Arthroscopy Thunderbolt System?

Responsive Arthroscopy Thunderbolt System is manufactured by Responsive Arthroscopy, LLC.

What is the FDA product code for Responsive Arthroscopy Thunderbolt System?

The FDA product code for Responsive Arthroscopy Thunderbolt System is MBI.

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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.

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