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
1301979092
Device Listing 1301979092
Listing Summary
#
Listing key
1301979092
Premarket submission
K094013
Device
HLS KNEETEC SYSTEM
Applicant
Tornier
Product code
JWH
Decision date
2011-05-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
95736
3000931034
3000931034
Tornier S.A.S.
1
N
2020-04-25
161 rue Lavoisier Montbonnot Saint-Martin Isere FR 38330