ClearanceBrief
510(k) K231701 ยท OWB Interventional Fluoroscopic X-Ray System

Ziehm Vision RFD 3D

ApplicantZiehm Imaging GmbH, Nuremberg, DE
DecisionSubstantially Equivalent, Jul 10, 2023
ReceivedJun 12, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K231701

DateFirm and productCodeLinked 510(k)
Dec 2, 2024Orthoscan, Inc.
Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system
Open, Classified
OWBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.