Medical Device Manufacturer · GB , Leeds

Depuy International, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Depuy International, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Leeds, GB.

Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by DePuy Orthopaedics, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Depuy International, Ltd.
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