HipCheck

System, Image Processing, Radiological

Stryker Corp.

The following data is part of a premarket notification filed by Stryker Corp. with the FDA for Hipcheck.

Pre-market Notification Details

Device IDK182359
510k NumberK182359
Device Name:HipCheck
ClassificationSystem, Image Processing, Radiological
Applicant Stryker Corp. 5900 Optical Ct San Jose,  CA  95138
ContactCara Mellits
CorrespondentCara Mellits
Stryker Corp. 5900 Optical Ct San Jose,  CA  95138
Product CodeLLZ  
CFR Regulation Number892.2050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-08-30
Decision Date2018-12-13
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
07613327459081 K182359 000

Trademark Results [HipCheck]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HIPCHECK
HIPCHECK
90894219 not registered Live/Pending
Stryker Corporation
2021-08-20
HIPCHECK
HIPCHECK
87694554 5822505 Live/Registered
Stryker Corporation
2017-11-22
HIPCHECK
HIPCHECK
87589656 5433281 Live/Registered
Francisco Avina
2017-08-30
HIPCHECK
HIPCHECK
78711206 3459414 Dead/Cancelled
The SCO Group, Inc.
2005-09-12
HIPCHECK
HIPCHECK
75439682 2209295 Dead/Cancelled
Ontario Corporation #1273313
1998-02-24

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