SI SOLUTIONS

FDA Device Registration & Listing · Columbia, MO, US · Registration 3042024509

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3042024509
FEI Number
3042024509
Entity Name
SI SOLUTIONS
City/State/Country
Columbia, MO, US
Establishment Address
1010 Club Village Dr Ste C, Columbia, MO 65203, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
SI Solutions (Owner Number: 10094337)
Owner / Operator Contact Address
1010 Club Village Dr, Suite C, Columbia, MO 65203, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

OPTUMSI SACROILIAC JOINT IMPLANT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUR Sacroiliac Joint Fixation Orthopedic Class 2 888.3040 2025-11-24

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SI Solutions
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K213667 SI-BONE, Inc. iFuse-TORQ® Implant System 2022-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042024509. Last updated year: 2026. Please use registration number 3042024509 when referencing this establishment in official correspondence.
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