FDA.reportPublic FDA data

STUCKENBROCK MEDIZINTECHNIK GMBH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96814523002808193STUCKENBROCK MEDIZINTECHNIK GMBH1N2020-04-25LESSINGSTRASSE 50 TUTTLINGEN Baden-Wurttemberg DE 78532

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
161911316082103K964880VARI-ANGLE HIP SCREW (VHS) SYSTEMKTT1997-10-16
161911991234436K171628HBS2 Headless Bone ScrewHWC2018-01-12
161911263313771K171624IXOS Radius Plate SystemHRS2018-03-29
161911530531249K011603VHS PEDIATRIC HIP SCREW SYSTEMKTT2001-08-15
161911034467511
161911060442494
161911163581582
161911669463392
161911674697846
161911683518398
161911718757715
161911732555506
161911850841023
161911866654864
161911915571313
161911955651082

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KTT22001-08-15
HRS12018-03-29
HWC12018-01-12

PMN#