FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Juliet® Ti LL Lumbar Interbody Device

K Number: K190877 · Decision May 29, 2019
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
44
Review Days
55

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Basic Information

Device Name
Juliet® Ti LL Lumbar Interbody Device
K Number
K190877
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spineart
Date Received
April 4, 2019
Decision Date
May 29, 2019
Product Code
OVD
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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