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
1512580220
Device Listing 1512580220
Listing Summary
#
Listing key
1512580220
Premarket submission
K143635
Device
KINETIS Total Knee System
Applicant
Mako Surgical
Product code
JWH
Decision date
2015-02-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
177670
3005985723
3005985723
MAKO SURGICAL CORP.
1
N
2020-04-25
2555 Davie Road Fort Lauderdale FL US 33317