JuggerKnot Soft Anchor
K-Number: K231128 · 2023-05-17
ApplicantRiverpoint Medical, LLC
Decision Date2023-05-17
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
JuggerKnot Soft Anchor is a medical device manufactured by Riverpoint Medical, LLC. It received FDA 510(k) clearance on 2023-05-17 under approval 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. It is manufactured by Riverpoint Medical, LLC. The 510(k) number is K231128.
When was JuggerKnot Soft Anchor approved by the FDA?
JuggerKnot Soft Anchor received FDA 510(k) clearance on 2023-05-17, under approval number K231128.
What company makes JuggerKnot Soft Anchor?
JuggerKnot Soft Anchor is manufactured by Riverpoint Medical, LLC.
What is the FDA product code for JuggerKnot Soft Anchor?
The FDA product code for JuggerKnot Soft Anchor is MBI.
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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.