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FDA 510(k)

iFuse Implant System® - iFuse-3D implant

K-Number: K162733 · 2017-03-10

ApplicantSI-BONE, Inc.
Decision Date2017-03-10
Product CodeOUR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

iFuse Implant System® - iFuse-3D implant is a medical device manufactured by SI-BONE, Inc.. It received FDA 510(k) clearance on 2017-03-10 under approval number K162733. The device is classified under product code OUR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the iFuse Implant System® - iFuse-3D implant?

iFuse Implant System® - iFuse-3D implant is a medical device that received FDA 510(k) clearance on 2017-03-10. It is manufactured by SI-BONE, Inc.. The 510(k) number is K162733.

When was iFuse Implant System® - iFuse-3D implant approved by the FDA?

iFuse Implant System® - iFuse-3D implant received FDA 510(k) clearance on 2017-03-10, under approval number K162733.

What company makes iFuse Implant System® - iFuse-3D implant?

iFuse Implant System® - iFuse-3D implant is manufactured by SI-BONE, Inc..

What is the FDA product code for iFuse Implant System® - iFuse-3D implant?

The FDA product code for iFuse Implant System® - iFuse-3D implant is OUR.

Related Clinical Trials

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Related PubMed Literature

PMID: 39892748 Long-term Safety and Performance of a Suprachoroidal Pressure Sensor System: Results of the EYEMATE-SC Trial Follow-up Study. Ophthalmology (2025) PMID: 41966145 From Registry to Reality: Opportunities to Enhance Post-market Surveillance of High-Risk Medical Devices Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review". International journal of health policy and management (2025) PMID: 39726899 How to improve the mechanical safety of a novel spinal implant while saving costs and time. JOR spine (2024)

Other Devices by SI-BONE, Inc.

K161893Neuromonitoring Kit K160652iFUSE Implant System K152681iFuse Implant System(R) K172268iFuse Implant System- iFuse Navigation K182983iFuse Implant System® K190230iFuse Implant System®

View all 22 devices →

Related Devices (Code: OUR)

K161755Integrity-SI TM Fusion SystemCoorstek Medical K153656PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd. K161210RIALTO(TM) SI Fusion System, Medtronic Reusable Instruments for Use with the IPC(TM) Powerease(TM) System, and Medtronic Navigated Manual Reusable Instruments for use with the StealthStation(TM) and IPC(TM) Powerease(TM) SystemsMedtronic Sofamor Danek K160652iFUSE Implant SystemSI-BONE, Inc. K152681iFuse Implant System(R)SI-BONE, Inc. K152237The Entasis Dual-Lead Sacroiliac ImplantCorelink, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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