Medical Device Manufacturer · US , Minneapolis , MN

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

1 submissions · 0 cleared · Since 1991

Total

Cleared

Denied

Orothmet, Inc. has 0 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 0 cleared submissions from 1991 to 1991. Primary specialty: Orthopedic.

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

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

1 devices

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