Medical Device Manufacturer · US , Madison , WI

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

2 submissions · 2 cleared · Since 1993
2
Total
2
Cleared
0
Denied

Arthrodyn, Inc. has 2 FDA 510(k) cleared medical devices. Based in Madison, US.

Historical record: 2 cleared submissions from 1993 to 1993. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Arthrodyn, Inc.
2 devices
1-2 of 2
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