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
1412980608
Device Listing 1412980608
Listing Summary
#
Listing key
1412980608
Premarket submission
K123890
Device
ACUMED CANNULATED SCREW SYSTEM
Applicant
Acumed, LLC
Product code
HWC
Decision date
2013-03-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
43243
3025141
1000125930
ACUMED LLC
1
Y
2026-01-01
5885 NE Cornelius Pass Rd Hillsboro OR US 97124