Devices

Device Recall Stryker PROFESS

Model / Serial
Lot #202085 Stryker Product Number: 6001-420-000
Product Classification
Ear, Nose, and Throat Devices
Device Class
2
Implanted device?
No
Distribution
US (nationwide) Distribution to the states of : CA, CT, GA, IL, IN, MA, MD, NC, OH, PA, TN, and TX.
Product Description
Stryker PROFESS Registration Kit. || The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a PROFESS Patient Tracker, and a PROFESS Adaptor Cable.
Manufacturer
Stryker Instruments Div. of Stryker Corporation
1 Event
- Recall of Device Recall Stryker PROFESS

Manufacturer

Stryker Instruments Div. of Stryker Corporation

Manufacturer Address
Stryker Instruments Div. of Stryker Corporation, 4100 E Milham Ave, Portage MI 49002-9704
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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