OrthoButton FL
K-Number: K202399 · 2020-09-18
ApplicantRiverpoint Medical
Decision Date2020-09-18
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
OrthoButton FL is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2020-09-18 under approval 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. It is manufactured by Riverpoint Medical. The 510(k) number is K202399.
When was OrthoButton FL approved by the FDA?
OrthoButton FL received FDA 510(k) clearance on 2020-09-18, under approval number K202399.
What company makes OrthoButton FL?
OrthoButton FL is manufactured by Riverpoint Medical.
What is the FDA product code for OrthoButton FL?
The FDA product code for OrthoButton FL 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.