FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

KHEIRON® Spinal Fixation System, including patient specific K-ROD

K Number: K260786 · Decision Apr 3, 2026
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
10
Review Days
24

Basic Information

Device Name
KHEIRON® Spinal Fixation System, including patient specific K-ROD
K Number
K260786
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
S.M.A.I.O
Date Received
March 10, 2026
Decision Date
April 3, 2026
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

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Other Clearances by S.M.A.I.O

K Number Device Name
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K232650 KHEIRON® Spinal Fixation System, including patient specific K-ROD
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