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
1448074900
Device Listing 1448074900
Listing Summary
#
Listing key
1448074900
Premarket submission
K023675
Device
SYNTHES CERVIFIX/ AXON
Applicant
Synthes (Usa)
Product code
KWP
Decision date
2002-11-26
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