Medical Device Manufacturer · CA , Notre-Dame-De-L'Lle-Perrot,Quebec

Porosteon, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014

Total

Cleared

Denied

Porosteon, Inc. has 1 FDA 510(k) cleared medical devices. Based in Notre-Dame-De-L'Lle-Perrot,Quebec, CA.

Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Porosteon, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Porosteon, Inc.

1 devices

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