Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Iconix® Anchor

K-Number: K241577 · 2024-07-03

ApplicantRiverpoint Medical
Decision Date2024-07-03
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Iconix® Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical. It received FDA 510(k) clearance on 2024-07-03 under 510(k) number K241577. 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® Anchor?

Iconix® Anchor is a medical device that received FDA 510(k) clearance on 2024-07-03. The listed applicant is Riverpoint Medical. The 510(k) number is K241577.

When did Iconix® Anchor receive FDA 510(k) clearance?

Iconix® Anchor received FDA 510(k) clearance on 2024-07-03, under 510(k) number K241577.

Who is the listed applicant for Iconix® Anchor?

The FDA 510(k) record lists Riverpoint Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Iconix® Anchor?

The FDA product code for Iconix® Anchor is MBI.

Other records listing Riverpoint Medical 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.

K253693Strut Suture; No-Tie ButtonK253695LigaMendK253024ProZip Knotless ImplantK252201HS FiberK252144Iconix Speed Anchor; Iconix Speed HA+ AnchorK243988RootMend MRR

View all 30 devices →

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.

K262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker EndoscopyK261770Suture Button Repair SystemSkeletal Dynamics, Inc.K261632Thunderbolt SystemResponsive Arthroscopy, Inc.K261968Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)Smith & Nephew, Inc.K260018Arthrex FiberButtonArthrex, Inc.

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.

↑