Medical Device Manufacturer · US , Plainview , NY

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

1 submissions · 1 cleared · Since 2017

Recent clearances: PHA S1 Spinal System

1
Total
1
Cleared
0
Denied

Phamedica, Inc. has 1 FDA 510(k) cleared medical devices. Based in Plainview, US.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Empirical Consulting, LLC as regulatory consultant.

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

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