FDA.reportPublic FDA data

CARTIVA, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30093511383009351138CARTIVA, INC.1N2020-04-256120 Windward Pkwy Ste 220 Alpharetta GA US 30005
30093511943009351194Cartiva, Inc.1N2020-04-251005 Alderman Dr Ste 208 Alpharetta GA US 30005

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1351031995579568P150017CARTIVA SYNTHETIC CARTILAGE IMPLANTPNW2016-07-01
1350961995579568P150017CARTIVA SYNTHETIC CARTILAGE IMPLANTPNW2016-07-01
1350961530153321K192156Cartiva SCI instrumentation setQBO2019-09-04
1351031530153321K192156Cartiva SCI instrumentation setQBO2019-09-04
1351031225013078K181348Cartiva SCI Disposable Instrumentation SetQBO2018-06-20
1350961225013078K181348Cartiva SCI Disposable Instrumentation SetQBO2018-06-20
1350961848802328K142490ProxiFuse Hammer Toe DeviceHWC2014-12-15
1350961840156317K121356MICRO/MINI N-PK(H) BONE ANCHORMBI2012-11-09
1350961052975352
1351031052975352
1350961156390654
1351031156390654
1350961892257295

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QBO42019-09-04
PNW22016-07-01
HWC12014-12-15
MBI12012-11-09

PMN#