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FDA 510(k)

OrthoButton AL

K-Number: K230212 · 2023-02-23

ApplicantRiverpoint Medical, LLC
Decision Date2023-02-23
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OrthoButton AL is the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical, LLC. It received FDA 510(k) clearance on 2023-02-23 under 510(k) number K230212. 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 2023-02-23. The listed applicant is Riverpoint Medical, LLC. The 510(k) number is K230212.

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

OrthoButton AL received FDA 510(k) clearance on 2023-02-23, under 510(k) number K230212.

Who is the listed applicant for OrthoButton AL?

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

What is the FDA product code for OrthoButton AL?

The FDA product code for OrthoButton AL is MBI.

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Related Devices (Code: MBI)

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K262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker EndoscopyK261770Suture Button Repair SystemSkeletal Dynamics, Inc.K261632Thunderbolt SystemResponsive Arthroscopy, Inc.K261968Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)Smith & Nephew, Inc.K260018Arthrex FiberButtonArthrex, Inc.

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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