PLACER

Stimulator, Spinal-cord, Implanted (pain Relief)

ADVANCED NEUROMODULATION SYSTEMS

The following data is part of a premarket notification filed by Advanced Neuromodulation Systems with the FDA for Placer.

Pre-market Notification Details

Device IDK032349
510k NumberK032349
Device Name:PLACER
ClassificationStimulator, Spinal-cord, Implanted (pain Relief)
Applicant ADVANCED NEUROMODULATION SYSTEMS 6501 WINDCREST DRIVE SUITE 100 Plano,  TX  75024
ContactKatryna Warren
CorrespondentKatryna Warren
ADVANCED NEUROMODULATION SYSTEMS 6501 WINDCREST DRIVE SUITE 100 Plano,  TX  75024
Product CodeGZB  
CFR Regulation Number882.5880 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-06-30
Decision Date2003-10-03

Trademark Results [PLACER]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PLACER
PLACER
97531295 not registered Live/Pending
County of Placer
2022-08-02
PLACER
PLACER
88607584 not registered Live/Pending
Trujillo, Martha Patricia
2019-09-06
PLACER
PLACER
88090878 5803740 Live/Registered
Placer Labs, Inc.
2018-08-23
PLACER
PLACER
86190445 4778176 Live/Registered
County of Placer
2014-02-11
PLACER
PLACER
85787549 4515674 Live/Registered
TAP Worldwide, LLC
2012-11-26
PLACER
PLACER
78904971 not registered Dead/Abandoned
A. V. Imports, Inc.
2006-06-09
PLACER
PLACER
78258871 not registered Dead/Abandoned
PBN Medicals Denmark A/S
2003-06-05
PLACER
PLACER
76516121 3139462 Dead/Cancelled
Advanced Neuromodulation Systems, Inc.
2003-05-21
PLACER
PLACER
75443508 not registered Dead/Abandoned
Medtronic, Inc.
1998-03-03
PLACER
PLACER
73580787 1411615 Dead/Cancelled
FIGI'S DATA CENTER, INC.
1986-02-03

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