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 ID | K182359 |
| 510k Number | K182359 |
| Device Name: | HipCheck |
| Classification | System, Image Processing, Radiological |
| Applicant | Stryker Corp. 5900 Optical Ct San Jose, CA 95138 |
| Contact | Cara Mellits |
| Correspondent | Cara Mellits Stryker Corp. 5900 Optical Ct San Jose, CA 95138 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-08-30 |
| Decision Date | 2018-12-13 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07613327459081 | K182359 | 000 |
Trademark Results [HipCheck]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HIPCHECK 90894219 not registered Live/Pending |
Stryker Corporation 2021-08-20 |
 HIPCHECK 87694554 5822505 Live/Registered |
Stryker Corporation 2017-11-22 |
 HIPCHECK 87589656 5433281 Live/Registered |
Francisco Avina 2017-08-30 |
 HIPCHECK 78711206 3459414 Dead/Cancelled |
The SCO Group, Inc. 2005-09-12 |
 HIPCHECK 75439682 2209295 Dead/Cancelled |
Ontario Corporation #1273313 1998-02-24 |
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