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

MODUS TRILOCK 2.0/2.3/2.5

K Number: K071612 · Decision Sep 11, 2007
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
42
Review Days
90

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Basic Information

Device Name
MODUS TRILOCK 2.0/2.3/2.5
K Number
K071612
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medartis AG
Date Received
June 13, 2007
Decision Date
September 11, 2007
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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