510(k) Report

Devices descending from K173702

2 later devices reach Juliet Ti LL through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K241321Juliet® Ti LL Lumbar Interbody DeviceSpineart SA20240—
+1K190877Juliet® Ti LL Lumbar Interbody DeviceSpineart201911