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
1216345540
Device Listing 1216345540
Listing Summary
#
Listing key
1216345540
Premarket submission
K173788
Device
Arthrex Corkscrew FT
Applicant
Arthrex, Inc.
Product code
MAI
Decision date
2018-03-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
295607
3010400367
3010400367
TRIBE MEDICAL GROUP
1
N
2026-01-01
595 Industrial Road London Ontario CA N5V 1V2