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

SQUALE

K Number: K230026 · Decision Mar 28, 2023
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
15
Review Days
83

Basic Information

Device Name
SQUALE
K Number
K230026
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implanet, S.A.
Date Received
January 4, 2023
Decision Date
March 28, 2023
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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