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

PEZO INTERBODY CAGES SYSTEM

K Number: K103814 · Decision Mar 17, 2011
Classifications
1
FEI Numbers
422
Registration Numbers
422
Same Product Code
869
Applicant Total
14
Review Days
78

Basic Information

Device Name
PEZO INTERBODY CAGES SYSTEM
K Number
K103814
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ULRICH GMBH & CO. KG
Date Received
December 29, 2010
Decision Date
March 17, 2011
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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