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
1312948322
Device Listing 1312948322
Listing Summary
#
Listing key
1312948322
Premarket submission
P030045
Device
INTRASTENT DOUBLESTRUT STENT
Applicant
MEDTRONIC VASCULAR INC
Product code
NIO
Decision date
2004-06-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
52258
2183870
2183870
ev3, Inc.
1
N
2026-01-01
4600 Nathan Lane North Plymouth MN US 55442