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

PEDIGUARD NERVE DETECTOR SYSTEM

K Number: K030526 · Decision Dec 29, 2004
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
12
Review Days
679

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Basic Information

Device Name
PEDIGUARD NERVE DETECTOR SYSTEM
K Number
K030526
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Vision, Inc.
Date Received
February 19, 2003
Decision Date
December 29, 2004
Product Code
GWF
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
GWF Stimulator, Electrical, Evoked Response

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Other Clearances by Spine Vision, Inc.

K Number Device Name
K052406 UNI-THREAD SPINAL SYSTEM
K042930 SPACEVISION CAGE SYSTEM
K042640 UNI-THREAD SPINAL SYSTEM
K033508 PLUS PIVOT LINK UNIVERSAL SYSTEM
K032398 PLUS PIVOT LINK UNIVERSAL SYSTEM
K022271 PLUS PIVOT LINK UNIVERSAL SYSTEM
K021507 PLUS PIVOT LINK UNIVERSAL SYSTEM
K021510 UNI-T UNI-THREAD SPINAL SYSTEM
K013301 UNI-T SPINAL SYSTEM
K013312 P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
Search all 12 clearances from Spine Vision, Inc. →