510(k) K230256

Device
Rebellion, Phantom Multi-Bite Kerrison Rongeur
Applicant
Morpheus AG
510(k) number
K230256
Product code
HAE
Decision
Substantially Equivalent (SESE)
Decision date
2023-03-03
Date received
2023-01-31
Regulation
882.4840
Classification name
Rongeur, Manual
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Dimitri Krutsch
Address
Bahnhofstraße 18 Spaichingen DE 78549 78549

FDA Registration Numbers

Source Documents

510(k) summary PDF

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