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510(k) Data Aggregation
K Number
K970706Manufacturer
Date Cleared
1997-05-22
(85 days)
Product Code
Regulation Number
888.3358Type
TraditionalPanel
OrthopedicReference & Predicate Devices
N/A
Why did this record match?
Device Name :
INTER-OP POROUS PROTRUSIO SHELL WITH SEALABLE SCREWHOLES
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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