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

Y-Knotless™ Flex Anchors

K Number: K253763 · Decision Jan 29, 2026
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
82
Review Days
65

Basic Information

Device Name
Y-Knotless™ Flex Anchors
K Number
K253763
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Conmed Corporation
Date Received
November 25, 2025
Decision Date
January 29, 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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