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

PREBENT PLATING WITH VIRTUAL SURGICAL PLANNING

K Number: K131674 · Decision Aug 8, 2013
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
25
Review Days
62

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Basic Information

Device Name
PREBENT PLATING WITH VIRTUAL SURGICAL PLANNING
K Number
K131674
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Microfixation
Date Received
June 7, 2013
Decision Date
August 8, 2013
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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