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
1737150366
Device Listing 1737150366
Listing Summary
#
Listing key
1737150366
Premarket submission
K063204
Device
SPIDERFX EMBOLIC PROTECTION DEVICE
Applicant
Ev3, Inc.
Product code
NTE
Decision date
2006-11-14
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