Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K072848
›
Descendants
Devices descending from K072848
3 later devices reach Activascrew through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K130716
Bioretec Activascrew Interference
Bioretec, Ltd.
2013
0
—
+1
K081392
Bioretec Activascrew, Activascrew Cannulated and Activascrew Cannulated with Activapin
Bioretec, Ltd.
2008
2
—
+2
K261057
ActivaScrew™ Cannulated COM
Bioretec, Ltd.
2026
0
—