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FDA 510(k)

JuggerKnot Soft Anchor

K-Number: K231128 · 2023-05-17

Decision Date2023-05-17
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

JuggerKnot Soft Anchor 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 2023-05-17 under 510(k) number K231128. 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 JuggerKnot Soft Anchor?

JuggerKnot Soft Anchor is a medical device that received FDA 510(k) clearance on 2023-05-17. The listed applicant is Riverpoint Medical, LLC. The 510(k) number is K231128.

When did JuggerKnot Soft Anchor receive FDA 510(k) clearance?

JuggerKnot Soft Anchor received FDA 510(k) clearance on 2023-05-17, under 510(k) number K231128.

Who is the listed applicant for JuggerKnot Soft Anchor?

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 JuggerKnot Soft Anchor?

The FDA product code for JuggerKnot Soft Anchor is MBI.

Other records listing Riverpoint Medical, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MBI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.