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

C-CURVE Interbody Fusion Device

K Number: K210470 · Decision Sep 3, 2021
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
25
Review Days
198

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Basic Information

Device Name
C-CURVE Interbody Fusion Device
K Number
K210470
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicrea International SA
Date Received
February 17, 2021
Decision Date
September 3, 2021
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

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