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

NERVE MONITORING CABLE

K Number: K073229 · Decision Jun 6, 2008
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
52
Applicant Total
50
Review Days
204

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Basic Information

Device Name
NERVE MONITORING CABLE
K Number
K073229
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
882.1350
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pioneer Surgical Technology
Date Received
November 15, 2007
Decision Date
June 6, 2008
Product Code
GXZ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXZ Electrode, Needle

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