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
1223137970
Device Listing 1223137970
Listing Summary
#
Listing key
1223137970
Premarket submission
K081586
Device
REPROCESSED EXTERNAL FIXATION DEVICE
Applicant
Sterilmed, Inc.
Product code
KTT
Decision date
2008-08-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17102
2134070
3001237663
STERILMED, INC.
1
N
2020-04-25
11400 73rd Ave N Ste 100 MAPLE GROVE MN US 55369
177649
3011276773
3011276773
STERILMED, INC.
1
N
2026-01-01
5010 Cheshire Pkwy N Ste 2 Plymouth MN US 55446