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

Aggeris™-C

K Number: K220182 · Decision Mar 30, 2022
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
10
Review Days
68

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Basic Information

Device Name
Aggeris™-C
K Number
K220182
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clariance
Date Received
January 21, 2022
Decision Date
March 30, 2022
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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