Cleared Special

K243323 - Iconix Knotless Anchor

K243323 is the FDA 510(k) clearance for Iconix Knotless Anchor by Riverpoint Medical. It is a Class 2 Orthopedic device (product code MBI) cleared through the Special 510(k) pathway after a 27-day FDA review.

K243323 · Riverpoint Medical · Orthopedic device
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Nov 2024
Decision
27d
Days
Class 2
Risk

K243323 is an FDA 510(k) clearance for the Iconix Knotless Anchor. Classified as Fastener, Fixation, Nondegradable, Soft Tissue within the MBI classification (a category for soft tissue fixation fasteners and anchoring systems), Class II - Special Controls.

Submitted by Riverpoint Medical (Portland, US). The FDA issued a Cleared decision on November 19, 2024 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - the FDA orthopedic device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Riverpoint Medical devices

Submission Details

510(k) Number K243323 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 23, 2024
Decision Date November 19, 2024
Days to Decision 27 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 122d · This submission: 27d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code MBI Fastener, Fixation, Nondegradable, Soft Tissue
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - MBI Fastener, Fixation, Nondegradable, Soft Tissue

All 390
Devices cleared under the same product code (MBI) and FDA review panel - the closest regulatory comparables to K243323.
Tigon Medical All-Suture Anchors (ASA)
K242529 · Tigon Medical · Dec 2024
Fix2Lock (PEEK Self Punching)
K243470 · Osteonic Co., Ltd. · Dec 2024
OsseoFit Interfacing Anchor
K242494 · Riverpoint Medical, LLC · Nov 2024
OC JuggerKnotless Soft Anchor
K243203 · Riverpoint Medical · Oct 2024
Extremity All Suture System
K241695 · Field Orthopaedics · Sep 2024
VersaTap™ Suture Anchor (ADP050)
K242296 · Ortho-Design (Pty), Ltd. · Aug 2024