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
1663810203
Device Listing 1663810203
Listing Summary
#
Listing key
1663810203
Premarket submission
K161417
Device
DePuy Synthes MAXFRAME Multi-Axial Correction System
Applicant
Synthes USA, LLC
Product code
KTT
Decision date
2016-11-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3812
3004464325
3004464325
DEPUY ORTHOPAEDICS
1
Y
2027-01-01
50 SCOTLAND BLVD. BRIDGEWATER MA US 02324