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FDA 510(k)

OC JuggerKnot Soft Anchor

K-Number: K240719 · 2024-04-11

Decision Date2024-04-11
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OC JuggerKnot Soft Anchor is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2024-04-11 under approval number K240719. 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 JuggerKnot Soft Anchor?

OC JuggerKnot Soft Anchor is a medical device that received FDA 510(k) clearance on 2024-04-11. It is manufactured by Riverpoint Medical. The 510(k) number is K240719.

When was OC JuggerKnot Soft Anchor approved by the FDA?

OC JuggerKnot Soft Anchor received FDA 510(k) clearance on 2024-04-11, under approval number K240719.

What company makes OC JuggerKnot Soft Anchor?

OC JuggerKnot Soft Anchor is manufactured by Riverpoint Medical.

What is the FDA product code for OC JuggerKnot Soft Anchor?

The FDA product code for OC JuggerKnot 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.