FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Unispace SA Cervical Cage

K Number: K213791 · Decision Aug 5, 2022
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
1
Review Days
242

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Basic Information

Device Name
Unispace SA Cervical Cage
K Number
K213791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Edisoninno Co., Ltd.
Date Received
December 6, 2021
Decision Date
August 5, 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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