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

CONCORDE CURVE SYSTEM

K Number: K103743 · Decision Mar 17, 2011
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
9
Review Days
84

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Basic Information

Device Name
CONCORDE CURVE SYSTEM
K Number
K103743
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Johnson & Johnson
Date Received
December 23, 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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