FDA.reportPublic FDA data

Oerlikon AM Medical Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
12255913000953487Oerlikon AM Medical Inc.1N2020-04-2510 Constitution Blvd S Shelton CT US 06484

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1508171980898082K192760NuVasive Modulus XLIF Interbody SystemMAX2019-10-18
1508171755895799K100757TILOCK PEDICLE SCREW SYSTEMNKB2010-07-01
1508171700577795K080402ENCORE SHOULDER PRIMARY HUMERAL STEM, MODEL 500-00, ENCORE SHOULDER HUMERAL HEAD, MODEL 520-38KWS2008-03-28
1508171872281480K060192APEX KNEE SYSTEMJWH2006-06-15
1508171403859508

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MAX12019-10-18
NKB12010-07-01
KWS12008-03-28
JWH12006-06-15