CAMBRIA

Intervertebral Fusion Device With Bone Graft, Cervical

SEASPINE, INC.

The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Cambria.

Pre-market Notification Details

Device IDK082309
510k NumberK082309
Device Name:CAMBRIA
ClassificationIntervertebral Fusion Device With Bone Graft, Cervical
Applicant SEASPINE, INC. 2302 LA MIRADA DR. Vista,  CA  92081 -7862
ContactJeff Brittan
CorrespondentJeff Brittan
SEASPINE, INC. 2302 LA MIRADA DR. Vista,  CA  92081 -7862
Product CodeODP  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2008-08-13
Decision Date2009-04-09
Summary:summary

NIH GUDID Devices

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Trademark Results [CAMBRIA]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CAMBRIA
CAMBRIA
98210440 not registered Live/Pending
Cambria Technologies, Inc.
2023-10-05
CAMBRIA
CAMBRIA
97818012 not registered Live/Pending
Cambria Company LLC
2023-03-01
CAMBRIA
CAMBRIA
90218242 not registered Live/Pending
Diono, LLC
2020-09-28
CAMBRIA
CAMBRIA
88472606 not registered Live/Pending
Stargrow Cultivar Development (Pty) Ltd.
2019-06-13
CAMBRIA
CAMBRIA
88043463 not registered Live/Pending
Cambria Company LLC
2018-07-18
CAMBRIA
CAMBRIA
87493292 5379380 Live/Registered
Pro-Tech Knives, LLC
2017-06-16
CAMBRIA
CAMBRIA
87408214 5334549 Live/Registered
Choice Hotels International, Inc.
2017-04-12
CAMBRIA
CAMBRIA
87317325 5261192 Live/Registered
Cambria Company LLC
2017-01-30
CAMBRIA
CAMBRIA
86629166 4873902 Live/Registered
Cambria beauty
2015-05-14
CAMBRIA
CAMBRIA
86161722 4611423 Live/Registered
Choice Hotels International, Inc.
2014-01-09
CAMBRIA
CAMBRIA
86161712 4611422 Live/Registered
Choice Hotels International, Inc.
2014-01-09
CAMBRIA
CAMBRIA
86049920 not registered Dead/Abandoned
Metal Networks, Inc.
2013-08-28

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