FDA.reportPublic FDA data

Pia Kim

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30142577763014257776Pia Kim1N2026-01-014020 215th St Bayside NY US 11361

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2175161591340164K241128TDM Plate and Screw SystemHRS2024-12-05
2175161766553350K240423TDM Anterior Cervical Plate SystemKWQ2024-04-08
2175161970284394K232115TDM Large Bone Plate and Screw SystemHRS2024-04-05
2175161319797406K231860TDM Screw SystemHWC2024-01-18
2175161154187959K230071Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus Interlocking Nail System, Tibia Interlocking Nail System, Compression Hip Nail SystemHSB2024-08-22
2175161301773629K221844TDM Lumbar Interbody Fusion Cage SystemMAX2022-08-17
2175161399773264K220285PINE Pedicle Screw SystemNKB2022-05-19
2175161576989146K191057Park's Pectus SystemHRS2020-03-19
2175161635601362K190830TDM Screw SystemsHWC2019-09-13
2175161423059447K190391TDM Plate and Screw SystemsHRS2019-11-15
2175161680697726K171808TDM Plate and Screw SystemHRS2018-03-15
2175161131086287
2175161187419131
2175161207375384
2175161257571888
2175161418956169
2175161710947554
2175161867711335
2175162034815657
2175162038859227
2175161423632233
2175161554225091
2175161630901738
2175161753085038
2175161892198544
2175161898105616
2175161952318721

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HRS72024-12-05
HWC32024-01-18
HSB12024-08-22
KWQ12024-04-08
MAX12022-08-17
NKB12022-05-19