Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1019063960
Device Listing 1019063960
Listing Summary
#
Listing key
1019063960
Premarket submission
K050934
Device
MODUS TITANIUM OSTEOSYNTHESIS SYSTEM
Applicant
Medartis, Inc.
Product code
JEY
Decision date
2005-05-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
54723
3003236702
3003236702
MEDARTIS AG
1
N
2026-01-01
HOCHBERGERSTRASSE 60E BASEL Basel-Stadt CH CH-4057