FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Iconix Speed Anchor; Iconix Speed HA+ Anchor

K Number: K252144 · Decision Jul 30, 2025
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
27
Review Days
22

Basic Information

Device Name
Iconix Speed Anchor; Iconix Speed HA+ Anchor
K Number
K252144
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Riverpoint Medical
Date Received
July 8, 2025
Decision Date
July 30, 2025
Product Code
MBI
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MBI Fastener, Fixation, Nondegradable, Soft Tissue

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Other Clearances by Riverpoint Medical

K Number Device Name
K253024 ProZip Knotless Implant
K252201 HS Fiber
K243323 Iconix Knotless Anchor
K243203 OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor
K241282 RibFix Titan™ Fixation System
K241577 Iconix® Anchor
K240719 OC JuggerKnot Soft Anchor
K240213 Iconix Knotless Anchor
K240194 ProCinch, QuadCinch
K231163 HS Fiber Sutures
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