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FDA 510(k)

OrthoButton FL

K-Number: K202399 · 2020-09-18

Decision Date2020-09-18
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OrthoButton FL is the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical. It received FDA 510(k) clearance on 2020-09-18 under 510(k) number K202399. 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 OrthoButton FL?

OrthoButton FL is a medical device that received FDA 510(k) clearance on 2020-09-18. The listed applicant is Riverpoint Medical. The 510(k) number is K202399.

When did OrthoButton FL receive FDA 510(k) clearance?

OrthoButton FL received FDA 510(k) clearance on 2020-09-18, under 510(k) number K202399.

Who is the listed applicant for OrthoButton FL?

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

What is the FDA product code for OrthoButton FL?

The FDA product code for OrthoButton FL is MBI.

Other records listing Riverpoint Medical 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.

View all 30 devices →

Related Devices (Code: MBI)

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.

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.