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

SYNTHES (USA) NEURO PLATE AND SCREW SYSTEM

K Number: K042365 · Decision Nov 18, 2004
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
288
Applicant Total
402
Review Days
79

Basic Information

Device Name
SYNTHES (USA) NEURO PLATE AND SCREW SYSTEM
K Number
K042365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SYNTHES (USA)
Date Received
August 31, 2004
Decision Date
November 18, 2004
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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