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
1816537443
Device Listing 1816537443
Listing Summary
#
Listing key
1816537443
Premarket submission
K071667
Device
SYNTHES VECTRA-ONE SYSTEM
Applicant
Synthes Spine
Product code
KWQ
Decision date
2007-11-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
163675
3009996808
3009996808
SYNTHES USA PRODUCTS, LLC
1
N
2020-04-25
325 Paramount Drive Raynham MA US 02767