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
1949474889
Device Listing 1949474889
Listing Summary
#
Listing key
1949474889
Premarket submission
K160568
Device
Precision Spine Interspinous Plate System
Applicant
Precision Spine, Inc.
Product code
PEK
Decision date
2016-05-04
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