Search Results
Found 1 results
510(k) Data Aggregation
K Number
K011206Manufacturer
Date Cleared
2001-07-18
(90 days)
Product Code
Regulation Number
876.1075Type
AbbreviatedReference & Predicate Devices
N/A
Why did this record match?
Device Name :
PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
Ask a Question
Ask a specific question about this device
Page 1 of 1