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

SPIRA® Anterior Lumbar Spacers

K Number: K234077 · Decision Jul 12, 2024
Classifications
1
FEI Numbers
422
Registration Numbers
422
Same Product Code
869
Applicant Total
14
Review Days
203

Basic Information

Device Name
SPIRA® Anterior Lumbar Spacers
K Number
K234077
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Camber Spine Technologies
Date Received
December 22, 2023
Decision Date
July 12, 2024
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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K190483 SPIRA Open Matrix ALIF and LLIF
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