Devices

Device Recall Scorpio Series 7000

Model / Serial
All Lot Codes
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide including the US and Asia Pacific, Canada, Europe, Middle East, Africa, Japan and Latin America.
Product Description
Scorpio Series 7000 Tibial Impactor/Extractor, Catalog number 3770-000 || Non Sterile || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || The Impactor/Extractor is used for insertion and removal of a tibial baseplate during total knee arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 Event
- Recall of Device Recall Scorpio Series 7000

Manufacturer

Stryker Howmedica Osteonics Corp.

Manufacturer Address
Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430-2002
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

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Disclaimer

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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