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

Arthrex Knee FiberTak® Button Suture Anchor

K Number: K232973 · Decision Nov 15, 2023
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
348
Review Days
55

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Basic Information

Device Name
Arthrex Knee FiberTak® Button Suture Anchor
K Number
K232973
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
September 21, 2023
Decision Date
November 15, 2023
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

Similar 510(k) Clearances

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Other Clearances by Arthrex, Inc.

K Number Device Name
K253931 Arthrex Bioabsorbable PushLock Suture Anchors
K254215 Arthrex Beaming System
K252016 Arthrex Humeral Nails
K260561 Arthrex FiberTak Suture Anchor
K260405 FiberTape Button
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
Search all 348 clearances from Arthrex, Inc. →