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

SIros-X System

K Number: K252322 · Decision Oct 22, 2025
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
130
Applicant Total
31
Review Days
89

Basic Information

Device Name
SIros-X System
K Number
K252322
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genesys Spine
Date Received
July 25, 2025
Decision Date
October 22, 2025
Product Code
OUR
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
OUR Sacroiliac Joint Fixation

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