Synergy Disc Replacement

FDA Filings

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

FDA Registration(s)
Registration Number3014213973
FEI Number3014213973
NameSynergy Disc Replacement
Owner & OperatorSynergy Disc Replacement
Contact Address357 S. McCaslin Blvd, Suite 120
Louisville CO 80027 US
Official Correspondent
  • Joshua Butters
  • 1-647-6923493-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address357 S McCaslin Blvd, Suite 120
Louisville, CO 80027 US
Establishment TypeManufacture Device in the United States for Export Only

FDA Filings

Device
Company
DeviceDate
Synergy Disc Replacement
Synergy Disc Surgical Instruments2018-01-03
Synergy Disc Replacement
Synergy Disc2017-12-22

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