Iconix Speed Anchor; Iconix Speed HA+ Anchor
K-Number: K252144 · 2025-07-30
ApplicantRiverpoint Medical
Decision Date2025-07-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Iconix Speed Anchor; Iconix Speed HA+ Anchor is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2025-07-30 under approval number K252144. 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 Iconix Speed Anchor; Iconix Speed HA+ Anchor?
Iconix Speed Anchor; Iconix Speed HA+ Anchor is a medical device that received FDA 510(k) clearance on 2025-07-30. It is manufactured by Riverpoint Medical. The 510(k) number is K252144.
When was Iconix Speed Anchor; Iconix Speed HA+ Anchor approved by the FDA?
Iconix Speed Anchor; Iconix Speed HA+ Anchor received FDA 510(k) clearance on 2025-07-30, under approval number K252144.
What company makes Iconix Speed Anchor; Iconix Speed HA+ Anchor?
Iconix Speed Anchor; Iconix Speed HA+ Anchor is manufactured by Riverpoint Medical.
What is the FDA product code for Iconix Speed Anchor; Iconix Speed HA+ Anchor?
The FDA product code for Iconix Speed Anchor; Iconix Speed HA+ 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.