The following data is part of a premarket notification filed by Advanced Neuromodulation Systems with the FDA for Placer.
Device ID | K032349 |
510k Number | K032349 |
Device Name: | PLACER |
Classification | Stimulator, Spinal-cord, Implanted (pain Relief) |
Applicant | ADVANCED NEUROMODULATION SYSTEMS 6501 WINDCREST DRIVE SUITE 100 Plano, TX 75024 |
Contact | Katryna Warren |
Correspondent | Katryna Warren ADVANCED NEUROMODULATION SYSTEMS 6501 WINDCREST DRIVE SUITE 100 Plano, TX 75024 |
Product Code | GZB |
CFR Regulation Number | 882.5880 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-06-30 |
Decision Date | 2003-10-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PLACER 97531295 not registered Live/Pending |
County of Placer 2022-08-02 |
PLACER 88607584 not registered Live/Pending |
Trujillo, Martha Patricia 2019-09-06 |
PLACER 88090878 5803740 Live/Registered |
Placer Labs, Inc. 2018-08-23 |
PLACER 86190445 4778176 Live/Registered |
County of Placer 2014-02-11 |
PLACER 85787549 4515674 Live/Registered |
TAP Worldwide, LLC 2012-11-26 |
PLACER 78904971 not registered Dead/Abandoned |
A. V. Imports, Inc. 2006-06-09 |
PLACER 78258871 not registered Dead/Abandoned |
PBN Medicals Denmark A/S 2003-06-05 |
PLACER 76516121 3139462 Dead/Cancelled |
Advanced Neuromodulation Systems, Inc. 2003-05-21 |
PLACER 75443508 not registered Dead/Abandoned |
Medtronic, Inc. 1998-03-03 |
PLACER 73580787 1411615 Dead/Cancelled |
FIGI'S DATA CENTER, INC. 1986-02-03 |