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

UNiD Spine Analyzer

K Number: K180091 · Decision Feb 8, 2018
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
17
Review Days
27

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Basic Information

Device Name
UNiD Spine Analyzer
K Number
K180091
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicrea International
Date Received
January 12, 2018
Decision Date
February 8, 2018
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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K140738 PASS LP SPINAL SYSTEM
K133906 C-JAWS CERVICAL COMPRESSIVE STAPLE
K132395 LIGAPASS
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K132575 PASS LP SPINAL SYSTEM
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