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FDA 510(k)

OrthoButton CL

K-Number: K160655 · 2016-06-03

Decision Date2016-06-03
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OrthoButton CL is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2016-06-03 under approval number K160655. 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 CL?

OrthoButton CL is a medical device that received FDA 510(k) clearance on 2016-06-03. It is manufactured by Riverpoint Medical. The 510(k) number is K160655.

When was OrthoButton CL approved by the FDA?

OrthoButton CL received FDA 510(k) clearance on 2016-06-03, under approval number K160655.

What company makes OrthoButton CL?

OrthoButton CL is manufactured by Riverpoint Medical.

What is the FDA product code for OrthoButton CL?

The FDA product code for OrthoButton CL 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.