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

MINI AND MICRO FRAGMENTS RECONSTRUCTION SYSTEM-NEOFACE

K Number: K102641 · Decision Dec 20, 2010
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
5
Review Days
98

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Basic Information

Device Name
MINI AND MICRO FRAGMENTS RECONSTRUCTION SYSTEM-NEOFACE
K Number
K102641
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neoortho Produtos Ortopedicos S/A
Date Received
September 13, 2010
Decision Date
December 20, 2010
Product Code
JEY
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JEY Plate, Bone

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K162874 Cannulated Screws Neoortho
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K132852 PEEK CAGE FOR THE VERTEBRAL SPINE
K113733 SMALL AND LARGE FRAGMENTS OSTEOSYNTHESIS SYSTEM NEOFIX