Nse Automatech

FDA Filings

This page includes the latest FDA filings for Nse Automatech. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009293341
FEI Number3009293341
NameMichael van de Woude
Owner & OperatorNSE-Automatech
Contact Address520 Rutherford
Granby CA-QC Quebec J2G 0B2 CA
Official Correspondent
  • Caroline Surprenant
  • 1-450-3787207-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2500 Bee Cave Road Bldg 1, Suite 300
Austin, TX 78746 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Michael van de Woude [NSE-Automatech]
iASSIST Knee System2013-02-07
Michael van de Woude [NSE-Automatech]
Navitrack OS Knee Universal2013-02-07
Michael van de Woude [NSE-Automatech]
Navitrack -Partial Hip Resurfacing2013-02-07
Michael van de Woude [NSE-Automatech]
Navitrack OS Unicond Knee Universal2013-02-07
Michael van de Woude [NSE-Automatech]
Navitrack OS Knee Universal2013-02-07
Michael van de Woude [NSE-Automatech]
Navitrack-CT Free Cup2013-02-07

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