FDA.reportPublic FDA data

Kathy Trier

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30130963183013096318Kathy Trier1N2020-04-2513465 Midway road Dallas TX US 75244
30142116183014211618Kathy Trier1N2020-04-2513465 Midway road Dallas TX US 75244

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2146711761820144K19220632mm Glenosphere and Humeral CupPHX2019-10-08
1946562044205736K19220632mm Glenosphere and Humeral CupPHX2019-10-08
2146711485106973K163669Humeris ShoulderPHX2017-05-17
1946561677315663K163669Humeris ShoulderPHX2017-05-17
1946561070765578K162455Humelock Reversed ShoulderPHX2017-01-17
2146711423851691K162455Humelock Reversed ShoulderPHX2017-01-17
2146711498107875K150488Humelock II Reversible Shoulder SystemPHX2015-11-13
1946561793709498K150488Humelock II Reversible Shoulder SystemPHX2015-11-13
1946561456837010K143721PRCT2HRS2015-08-27
1946561316683051K140071HUMELOCK II CEMENTED SHOULDER SYSTEMKWT2014-07-28
2146711335856758K130759HUMELOCK II CEMENTLESS SHOULDER SYSTEMHSD2013-11-09
1946561772365598K130759HUMELOCK II CEMENTLESS SHOULDER SYSTEMHSD2013-11-09
2146711180922223K123814HUMELOCK II CEMENTED SHOULDER SYSTEMKWT2013-08-13
1946561188422141K123814HUMELOCK II CEMENTED SHOULDER SYSTEMKWT2013-08-13
1946561286024551K111097HUMELOCK CEMENTED SHOULDER PROSTHESISHSD2011-11-09
1946561823427184

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PHX82019-10-08
KWT32014-07-28
HSD32013-11-09
HRS12015-08-27