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FDA 510(k)

OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor

K-Number: K243203 · 2024-10-29

Decision Date2024-10-29
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2024-10-29 under approval number K243203. 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 OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor?

OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor is a medical device that received FDA 510(k) clearance on 2024-10-29. It is manufactured by Riverpoint Medical. The 510(k) number is K243203.

When was OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor approved by the FDA?

OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor received FDA 510(k) clearance on 2024-10-29, under approval number K243203.

What company makes OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor?

OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor is manufactured by Riverpoint Medical.

What is the FDA product code for OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor?

The FDA product code for OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor 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.