FDA.reportPublic FDA data

Nuvectra Corporation

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30099201613009920161Nuvectra Corporation1N2020-04-25105 Edgeview Dr Ste 310 Broomfield CO US 80021
30103098403010309840Nuvectra Corporation1N2020-04-2510675 Naples St NE Minneapolis MN US 55449
30118746923011874692Nuvectra Corporation1N2020-04-255830 Granite Parkway, Suite 1100 Plano TX US 75024

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1927671504515116P130028ALGOVITA SPINAL CORD STIMULATION SYSTEMLGW2015-11-20
1927691504515116P130028ALGOVITA SPINAL CORD STIMULATION SYSTEMLGW2015-11-20
1927381504515116P130028ALGOVITA SPINAL CORD STIMULATION SYSTEMLGW2015-11-20

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LGW32015-11-20

PMA#