Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K211689
›
Descendants
Devices descending from K211689
2 later devices reach KEYSTONE PEEK Cage System through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K254017
SWINGO-3D Lumbar Cage System
Implanet
2026
0
—
+1
K230872
Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™ Direction…
Shanghai Sanyou Medical Co, Ltd.
2023
1
—