JuggerKnot Soft Anchor OC
K-Number: K232411 · 2023-10-06
ApplicantRiverpoint Medical, LLC
Decision Date2023-10-06
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
JuggerKnot Soft Anchor OC is a medical device manufactured by Riverpoint Medical, LLC. It received FDA 510(k) clearance on 2023-10-06 under approval number K232411. 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 OC?
JuggerKnot Soft Anchor OC is a medical device that received FDA 510(k) clearance on 2023-10-06. It is manufactured by Riverpoint Medical, LLC. The 510(k) number is K232411.
When was JuggerKnot Soft Anchor OC approved by the FDA?
JuggerKnot Soft Anchor OC received FDA 510(k) clearance on 2023-10-06, under approval number K232411.
What company makes JuggerKnot Soft Anchor OC?
JuggerKnot Soft Anchor OC is manufactured by Riverpoint Medical, LLC.
What is the FDA product code for JuggerKnot Soft Anchor OC?
The FDA product code for JuggerKnot Soft Anchor OC 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.