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FDA 510(k) Applications Submitted by JOHN ROSS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K202186
08/04/2020
TrueRelief Device
TrueRelief
K190691
03/18/2019
Pixx2430 Digital Diagnostic X-Ray Receptor Panel
Pixxgen Corporation
K180976
04/13/2018
PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels
Pixxgen Corporation
K201172
05/01/2020
CFP-3131, CFP-2222
MX Imaging, Inc.
K152151
08/03/2015
ATAL 9
ATLAIM CORPORATION
K102284
08/12/2010
KRYSTALRAD 560 (FLAATZ 560)
MEDICATECH USA
K102285
08/12/2010
KRYSTALRAD (ATAL8)
MEDICATECH USA
K182533
09/14/2018
PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels
Pixxgen Corporation
K161173
04/26/2016
Avenue« T TLIF Cage
LDR SPINE USA, INC.
K163621
12/22/2016
Vitoss Bioactive (BA) Injectable
Orthovita, Inc.
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