FDA.report

510(k) K233172

Device
NextAR™ Spine Platform
Applicant
Medacta International S.A.
510(k) number
K233172
Product code
SBF
Decision
Substantially Equivalent (SESE)
Decision date
2024-04-24
Date received
2023-09-28
Regulation
882.4560
Classification name
Orthopedic Augmented Reality
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Stefano Baj
Address
Strada Regina Castel San Pietro (Ch) CH CH-6874 CH-6874

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code SBF

510(k)DeviceApplicantDecision date
K253805Knee+Pixee Medical S.A.S.2026-04-24
K252847NextAR Hip PlatformMedacta International S.A.2026-01-09
K251639xvision Spine systemAugmedics, Ltd.2025-10-03
K252054SpineAR SNAP (SyncAR Spine)Surgical Theater, Inc.2025-09-29
K252530OptiVu™ ShoulderMr Surgical Solutions, LLC2025-09-10
K251737NextAR(TM) Shoulder PlatformMedacta International S.A.2025-09-04
K252170OptiVu™ ShoulderMr Surgical Solutions, LLC2025-08-08
K250477NextAR(TM) SpineMedacta International S.A.2025-07-31
K250108OptiVu™ ShoulderMr Surgical Solutions, LLC2025-07-09
K241525ExcelsiusXR™Globus Medical, Inc.2025-07-08
K242569Mixed Reality Spine NavigationBrainlab AG2025-05-16
K243980ARVIS Surgical Navigation SystemKico Knee Innovation Company Pty Limited2025-03-21
K243975Knee+Pixee Medical2025-03-20
K250255xvision Spine systemAugmedics, Ltd.2025-03-13
K243950ARVIS® ShoulderKico Knee Innovation Company Pty, Ltd.2025-01-13