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
1991617489
Device Listing 1991617489
Listing Summary
#
Listing key
1991617489
Premarket submission
K231857
Device
Arthrex TightRope II
Applicant
Arthrex, Inc.
Product code
MBI
Decision date
2023-08-08
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