Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K060808
›
Descendants
Devices descending from K060808
3 later devices reach Brainpro, Brainpro Access through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K220897
Disposable Brain Biopsy Needle 2.0
PAJUNK GmbH Medizintechnologie
2022
1
—
+1
K112094
Brain Biopsy Needle
Ad-Tech Medical Instrument Corp
2012
0
—
+2
K230201
Disposable Pre-calibrated Brain Biopsy Needle 2.0
PAJUNK GmbH Medizintechnologie
2023
0
—