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

DYNEX® External Fixation Systems

K Number: K260900 · Decision Apr 17, 2026
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
17
Review Days
30

Basic Information

Device Name
DYNEX® External Fixation Systems
K Number
K260900
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vilex, LLC
Date Received
March 18, 2026
Decision Date
April 17, 2026
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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