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
1489618174
Device Listing 1489618174
Listing Summary
#
Listing key
1489618174
Premarket submission
K161755
Device
Integrity-SI TM Fusion System
Applicant
Coorstek Medical
Product code
OUR
Decision date
2016-12-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
78148
3004086872
3004086872
Lincotek Medical
1
N
2020-04-25
867 W. 400 N. Logan UT US 84321