Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K100353
›
Descendants
Devices descending from K100353
3 later devices reach Spinewand Surgical Device through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K162490
Disc-FX System
Elliquence, LLC
2017
0
—
+1
K132099
Arthrocare Coblator IQ DLR Spinewand, Arthrocare Coblator IQ DLG Spinewand
ArthroCare Corporation
2013
1
—
+2
K150915
Spinaut-P
Imedicom Co., Ltd.
2016
0
—