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
1848251695
Device Listing 1848251695
Listing Summary
#
Listing key
1848251695
Premarket submission
K231232
Device
Curiteva Laminoplasty System
Applicant
Curiteva, Inc.
Product code
NQW
Decision date
2023-06-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
188240
3012131184
3012131184
CURITEVA, INC.
1
N
2026-01-01
25127 WILL MCCOMB DR Tanner AL US 35671