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

Tigon Medical Knotless and Dual Javelin All-Suture Anchors

K Number: K252596 · Decision Dec 4, 2025
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
7
Review Days
111

Basic Information

Device Name
Tigon Medical Knotless and Dual Javelin All-Suture Anchors
K Number
K252596
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tigon Medical
Date Received
August 15, 2025
Decision Date
December 4, 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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K Number Device Name
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K240175 Tigon Medical Fractures, Instability, and Reconstruction (FIRE)
K220464 Tigon Medical Gryphon Anchor Line
K211049 Tigon Medical Button System
K182507 Tigon Medical Tissue Anchors