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

Arthrex FiberTak Suture Anchor

K Number: K260561 · Decision Mar 20, 2026
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
348
Review Days
29

Basic Information

Device Name
Arthrex FiberTak Suture Anchor
K Number
K260561
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
February 19, 2026
Decision Date
March 20, 2026
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 Arthrex, Inc.

K Number Device Name
K253931 Arthrex Bioabsorbable PushLock Suture Anchors
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K252016 Arthrex Humeral Nails
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K252196 Arthrex FibuLock Nail System
K260353 Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button
K254229 Arthrex Nano FiberTak Suture Anchor
K253713 Arthrex Variable Angle (VA) Proximal Tibia Plating System
K252807 Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
K253895 Arthrex SwiveLock Suture Anchor, 3.5 x 10 mm
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