Devices

Device Recall RIO THA System

Model / Serial
Part Item #: 204863 - THA 1.0 Application User Guide Part Item #: 207116 - THA 2.0 Application User Guide Part Item #: 208692 - THA 2.1 Application User Guide Part Item #: 209711 - MAKOplasty THA Application User Guide Part Item #: 210555 - MAKIplast THA 3.1 Application User Guide Part Item#: 212026 - THA Application User Guide 2.1-2.1.1 THA 3.0, THA 3.1, 3.1.1 and 3.1.1.1 Part Item # 204863 THA 1.0 Application User Guide Part Item # 207116 THA 2.0 Application User Guide Part Item # 208692 THA 2.1 Application User Guide Part Item # 209711 MAKOplasty THA Application User Guide Part Item # 210555 MAKIplast THA 3.1 Application User Guide Part Item # 212026 THA Application User Guide
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
No
Distribution
US nationwide distribution.
Product Description
MAKO RIO THA Application User Guides, for total hip arthroplasty, orthopedic surgery.
Manufacturer
Mako Surgical Corporation
1 Event
- Recall of Device Recall RIO THA System

Manufacturer

Mako Surgical Corporation

Manufacturer Address
Mako Surgical Corporation, 2555 Davie Rd Ste 110, Davie FL 33317-7424
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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