This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial.This project was partially supported by Pew Charitable Trusts and by the US Food and Drug Administration through grant 1U01FD005478.Publishe
This is an open access article distributed in accordance with the Creative Commons Attribution Non C...
textabstractRecent safety issues involving non-active implantable medical devices (NAIMDs) have high...
The recent catastrophe of metal-on-metal Total Hip Arthroplasty devices have highlighted the need fo...
This is an open access article distributed in accordance with the Creative Commons Attribution Non C...
Purpose: Recent safety issues involving medical devices have highlighted the need for better postmar...
Medical device manufacturers must continuously evaluate all clinical data available for their produc...
It is estimated that at this moment approximately 500,000 different medical devices are marketed in ...
Objective: To evaluate the FDA’s approval process and postmarket surveillance strategies for THR dev...
Background Following the public healthcare scandal surrounding Poly Implant Prothèse breast implants...
BACKGROUND The process of assuring the safety of medical devices is constrained by reliance on volun...
Background—Postmarket medical device surveillance in the United States depends largely on voluntary ...
Background: Recent safety issues involving medical devices have highlighted the need for better safe...
Managing medical device monitoring processes is challenging and lacks a realtime, life cycle trackin...
Abstract Background The serious adverse events associated with metal on metal hip replacements have ...
Modern Implantable Medical Devices (IMDs), implement capabilities that have contributed significantl...
This is an open access article distributed in accordance with the Creative Commons Attribution Non C...
textabstractRecent safety issues involving non-active implantable medical devices (NAIMDs) have high...
The recent catastrophe of metal-on-metal Total Hip Arthroplasty devices have highlighted the need fo...
This is an open access article distributed in accordance with the Creative Commons Attribution Non C...
Purpose: Recent safety issues involving medical devices have highlighted the need for better postmar...
Medical device manufacturers must continuously evaluate all clinical data available for their produc...
It is estimated that at this moment approximately 500,000 different medical devices are marketed in ...
Objective: To evaluate the FDA’s approval process and postmarket surveillance strategies for THR dev...
Background Following the public healthcare scandal surrounding Poly Implant Prothèse breast implants...
BACKGROUND The process of assuring the safety of medical devices is constrained by reliance on volun...
Background—Postmarket medical device surveillance in the United States depends largely on voluntary ...
Background: Recent safety issues involving medical devices have highlighted the need for better safe...
Managing medical device monitoring processes is challenging and lacks a realtime, life cycle trackin...
Abstract Background The serious adverse events associated with metal on metal hip replacements have ...
Modern Implantable Medical Devices (IMDs), implement capabilities that have contributed significantl...
This is an open access article distributed in accordance with the Creative Commons Attribution Non C...
textabstractRecent safety issues involving non-active implantable medical devices (NAIMDs) have high...
The recent catastrophe of metal-on-metal Total Hip Arthroplasty devices have highlighted the need fo...