FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

CINA-CSpine

K Number: K240942 · Decision Sep 12, 2024
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
85
Applicant Total
7
Review Days
160

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Basic Information

Device Name
CINA-CSpine
K Number
K240942
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2080
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avicenna.Ai
Date Received
April 5, 2024
Decision Date
September 12, 2024
Product Code
QAS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QAS Radiological Computer-Assisted Triage And Notification Software

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QAS), ordered by most recent decision date.

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Other Clearances by Avicenna.Ai

K Number Device Name
K240612 CINA-VCF
K233342 CINA-ASPECTS
K233968 CINA-iPE
K221716 CINA
K210237 CINA CHEST
K200855 CINA