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
1836942261
Device Listing 1836942261
Listing Summary
#
Listing key
1836942261
Premarket submission
K213394
Device
Vy Spine™ VySpan™ PCT System
Applicant
Vy Spine, LLC
Product code
NKG
Decision date
2021-12-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
294654
3019837678
3019837678
VY SPINE, LLC
1
N
2026-01-01
545 West 500 South Suite 100 & 110 Bountiful UT US 84010