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

AESCULAP CRANIOFACIAL PLATE AND SCREW

K Number: K060492 · Decision Apr 7, 2006
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
207
Review Days
42

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Basic Information

Device Name
AESCULAP CRANIOFACIAL PLATE AND SCREW
K Number
K060492
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap, Inc.
Date Received
February 24, 2006
Decision Date
April 7, 2006
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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