510(k) Report

Devices descending from K123207

16 later devices reach Primalif TM Llif Unitary Peek Lateral Lumbar Interbody Fusion System through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K160976Altus Spine Interbody Fusion SystemAltus Partners, LLC20178—
+1K131540Interfuse L Intervertebral Body Fusion DeviceVertebral Technologies, Inc.20136—
+2K182406Altus Spine Interbody Fusion SystemAltus Partners, LLC20191—
+2K170553Altus Spine Interbody Fusion SystemAltus Partners, LLC20170—
+2K171329Altus Spine Titanium Interbody Fusion SystemAltus Partners, LLC20172—
+2K170512Altus Spine Titanium Interbody Fusion SystemAltus Partners, LLC20176—
+2K160074Rampart D Lumbar Interbody Fusion DeviceSpineology, Inc.20165—
+3K211837Altus Spine Interbody Standalone Fusion SystemAltus Partners, LLC20220—
+3K181829Velofix TLIF CageU&I Corporation20181—
+3K172253Altus Spine Cervical Interbody Fusion SystemAltus Partners, LLC20170—
+3K171660Duo Lumbar Interbody Fusion DeviceSpineology, Inc.20174—
+4K183243Velofix TLIF CageU&I Corporation20190—
+4K181792Duo™ Lumbar Interbody Fusion DeviceSpineology, Inc.20183—
+5K190055Duo Lumbar Interbody Fusion DeviceSpineology, Inc.20191—
+5K182322Duo Lumbar Interbody Fusion DeviceSpineology, Inc.20182—
+6K210155Duo Expandable Interbody Fusion SystemSpineology, Inc.20210—