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
1538103418
Device Listing 1538103418
Listing Summary
#
Listing key
1538103418
Premarket submission
K182470
Device
Plateau Spacer System
Applicant
Life Spine
Product code
MAX
Decision date
2018-11-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
63214
3004499989
3004499989
LIFE SPINE
1
N
2020-04-25
13951 S Quality Drive Huntley IL US 60142
345405
3004499989
3004499989
LIFE SPINE
1
Y
2026-01-01
13951 Quality Dr Huntley IL US 60142