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
1658401035
Device Listing 1658401035
Listing Summary
#
Listing key
1658401035
Premarket submission
K163670
Device
Rampart One Lumbar Interbody Fusion Device
Applicant
Spineology, Inc.
Product code
OVD
Decision date
2017-05-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
56014
2135156
3003179719
SPINEOLOGY INC.
1
N
2026-01-01
7800 THIRD STREET N. SUITE 600 Saint Paul MN US 55128