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
1112825498
Device Listing 1112825498
Listing Summary
#
Listing key
1112825498
Premarket submission
K173130
Device
ReformĀ® Midline Cortical Screw System
Applicant
Precision Spine, Inc.
Product code
NKB
Decision date
2017-12-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
66754
3005739886
3005739886
Precision Spine, Inc.
1
N
2026-01-01
2050 Executive Dr Pearl MS US 39208