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

SYNTHES MATRIXMANDIBLE PERFORMED RECONSTRUCTION PLATES

K Number: K113251 · Decision Dec 21, 2011
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
8
Review Days
48

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Basic Information

Device Name
SYNTHES MATRIXMANDIBLE PERFORMED RECONSTRUCTION PLATES
K Number
K113251
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes, Inc.
Date Received
November 3, 2011
Decision Date
December 21, 2011
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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Other Clearances by Synthes, Inc.

K Number Device Name
K131792 SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY
K122647 SYNTHES PATIENT SPECIFIC PLATE
K113567 SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM
K121502 SYNTHES CURVILINEAR DISTRACTION SYSTEM
K121574 SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM
K111323 SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS
K112689 SYNTHES STERNAL FIXATION SYSTEM