510(k) K221949

Device
Ortho Device, ADAPTIX 3D Orthopedic Imaging System
Applicant
Pausch Medical GmbH
510(k) number
K221949
Product code
IZF
Decision
Substantially Equivalent (SESE)
Decision date
2023-01-26
Date received
2022-07-05
Regulation
892.1740
Classification name
System, X-Ray, Tomographic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Christian Stoian
Address
Graf-Zeppelin-Strabe 1 Erlangen DE D-91056 D-91056

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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K132261DISCOVERY XR656 WITH VOLUMERAD (DIGITAL TOMOSYNTHESIS)Ge Medical Systems, LLC2013-11-18
K121499FUJIFILM TOMOSYNTHESIS OPTION FOR FDR ACSELERATE STATIONARY X-RAY SYSTEMFujifilm Medical System U.S.A., Inc.2012-11-20
K013620MEDSTONE, UROPRO 2000, TOMOGRAPHIC OPTIONMedstone Intl., Inc.2002-01-22
K011290PROGNOST ES, MODEL 0302 0000Xmar Corp.2001-05-30
K973864COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMOPausch Corp.1998-06-17
K973834CS2000 & CS2000 TOMOPausch Corp.1998-04-30
K950571LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270Continental X-Ray Corp.1995-03-31