Medical Device Manufacturer · US , Lone Tree , CO

Inter-Os Technologies - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Inter-Os Technologies has 1 FDA 510(k) cleared medical devices. Based in Lone Tree, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Orthopedic.

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FDA 510(k) Regulatory Record - Inter-Os Technologies

1 devices

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