Medical Device Manufacturer · DE , Spaichingen

Morpheus AG - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2021
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Morpheus AG Neurology ✕
3 devices
1-3 of 3
Cleared Mar 03, 2023
Rebellion, Phantom Multi-Bite Kerrison Rongeur
K230256 · HAE
Neurology · 31d
Cleared Oct 07, 2022
Rebellion
K221818 · HAE
Neurology · 106d
Cleared May 04, 2021
Rebellion, Phantom Multi-Bite Kerrison Rongeur 
K200768 · HAE
Neurology · 405d
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All3 Neurology 3