K241574

iFuse TORQ® Implant System

510(k) number
K241574
Device name
iFuse TORQ® Implant System
Applicant
SI-BONE, Inc. CA · US
Product code
OUR — Sacroiliac Joint Fixation
Decision date
2024-07-02
Date received
2024-06-03
Decision
Substantially Equivalent
Clearance type
Special
Advisory committee
Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain

Also available from FDA: K241574.pdf

Official FDA record: K241574
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.