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
1712526482
Device Listing 1712526482
Listing Summary
#
Listing key
1712526482
Premarket submission
K071438
Device
PSS SYSTEM
Applicant
Spinal USA
Product code
MNI
Decision date
2007-08-21
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