Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K170341
›
Descendants
Devices descending from K170341
4 later devices reach Medussa-PL Cage through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K223654
Medussa-PL Cage
Medyssey USA, Inc.
2022
0
—
+1
K200283
Medussa-PL Cage
Medyssey USA, Inc.
2020
0
—
+1
K180990
TirboLOX-L Lumbar IBFD
Captiva Spine, Inc.
2018
1
—
+2
K181229
TirboLOX-C Cervical IBFD
Captiva Spine, Inc.
2018
0
—