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

HS Fiber

K Number: K252201 · Decision Aug 13, 2025
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
27
Review Days
30

Basic Information

Device Name
HS Fiber
K Number
K252201
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.5000
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Riverpoint Medical
Date Received
July 14, 2025
Decision Date
August 13, 2025
Product Code
GAT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

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K Number Device Name
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K252144 Iconix Speed Anchor; Iconix Speed HA+ Anchor
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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