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FDA 510(k)

OrthoButton AL

K-Number: K171060 · 2017-06-02

Decision Date2017-06-02
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OrthoButton AL is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2017-06-02 under approval number K171060. 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 AL?

OrthoButton AL is a medical device that received FDA 510(k) clearance on 2017-06-02. It is manufactured by Riverpoint Medical. The 510(k) number is K171060.

When was OrthoButton AL approved by the FDA?

OrthoButton AL received FDA 510(k) clearance on 2017-06-02, under approval number K171060.

What company makes OrthoButton AL?

OrthoButton AL is manufactured by Riverpoint Medical.

What is the FDA product code for OrthoButton AL?

The FDA product code for OrthoButton AL is MBI.

Other Devices by Riverpoint Medical

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Related Devices (Code: MBI)

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.