FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

TITANIUM MANDIBULAR FRACTURE SYSTEM

K Number: K952168 · Decision Jun 22, 1995
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
14
Review Days
45

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Basic Information

Device Name
TITANIUM MANDIBULAR FRACTURE SYSTEM
K Number
K952168
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicon, Inc.
Date Received
May 8, 1995
Decision Date
June 22, 1995
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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