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FDA 510(k)

OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct

K-Number: K242494 · 2024-11-26

ApplicantRiverpoint Medical, LLC
Decision Date2024-11-26
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct is a medical device manufactured by Riverpoint Medical, LLC. It received FDA 510(k) clearance on 2024-11-26 under approval number K242494. 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 OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct?

OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct is a medical device that received FDA 510(k) clearance on 2024-11-26. It is manufactured by Riverpoint Medical, LLC. The 510(k) number is K242494.

When was OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct approved by the FDA?

OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct received FDA 510(k) clearance on 2024-11-26, under approval number K242494.

What company makes OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct?

OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct is manufactured by Riverpoint Medical, LLC.

What is the FDA product code for OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct?

The FDA product code for OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct is MBI.

Related Clinical Trials

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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.

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