All-Suture Anchor
K-Number: K231078 · 2023-10-05
ApplicantRiverpoint Medical, LLC
Decision Date2023-10-05
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
All-Suture Anchor is a medical device manufactured by Riverpoint Medical, LLC. It received FDA 510(k) clearance on 2023-10-05 under approval number K231078. 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 All-Suture Anchor?
All-Suture Anchor is a medical device that received FDA 510(k) clearance on 2023-10-05. It is manufactured by Riverpoint Medical, LLC. The 510(k) number is K231078.
When was All-Suture Anchor approved by the FDA?
All-Suture Anchor received FDA 510(k) clearance on 2023-10-05, under approval number K231078.
What company makes All-Suture Anchor?
All-Suture Anchor is manufactured by Riverpoint Medical, LLC.
What is the FDA product code for All-Suture Anchor?
The FDA product code for All-Suture Anchor is MBI.
Other Devices by Riverpoint Medical, LLC
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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.