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510(k) Data Aggregation
K Number
K251863Device Name
CustomSurg OrthoPlanner
Manufacturer
CustomSurg AG
Date Cleared
2025-07-07
(20 days)
Product Code
LLZ
Regulation Number
892.2050Why did this record match?
Applicant Name (Manufacturer) :
CustomSurg AG
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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