FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

F3D-C2 Cervical Stand-Alone System

K Number: K211417 · Decision Feb 4, 2022
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
35
Review Days
273

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Basic Information

Device Name
F3D-C2 Cervical Stand-Alone System
K Number
K211417
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corelink, LLC
Date Received
May 7, 2021
Decision Date
February 4, 2022
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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