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

RENEW NEUROSTIMULATION SYSTEM

K Number: K000852 · Decision Jan 19, 2001
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
23
Applicant Total
25
Review Days
310

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Basic Information

Device Name
RENEW NEUROSTIMULATION SYSTEM
K Number
K000852
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Advanced Neuromodulation Systems
Date Received
March 15, 2000
Decision Date
January 19, 2001
Product Code
GZF
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
GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GZF), ordered by most recent decision date.

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Other Clearances by Advanced Neuromodulation Systems

K Number Device Name
K092371 SWIFT-LOCK ANCHOR, MODEL 1192
K090907 PENTA LEAD KITS, MODELS: 3227-3234
K081208 CINCH ANCHOR, MODEL 1194
K072462 WIDE SPACED QUATTRODE LEADS
K070847 TRIAL CABLE, 3009
K063080 TRIPOLE 8C AND 16C AND EXCLAIM 8 LAMITRODE SERIES LEADS
K053250 ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT
K052374 RAPID PROGEAMMER 3.0
K052418 AXXESS BUTTERFLY ANCHOR
K050922 ANS SCS ACCESSORY KIT
Search all 25 clearances from Advanced Neuromodulation Systems →