SIGN IM NAIL

INTRAMEDULLARY ROD

This device is manufactured by SIGN FRACTURE CARE INTERNATIONAL, SIGN FRACTURE CARE INTL.

The following problems were reported about this device:

Year Description Events/year Type
2024 Post Operative Wound Infection 3 Patient
2024 Limb Fracture 38 Patient
2024 Break 5 Device
2024 Adverse Event Without Identified Device or Use Problem 23 Device
2023 Post Operative Wound Infection 6 Patient
2023 Limb Fracture 38 Patient
2023 Migration 1 Device
2023 Break 8 Device
2023 Adverse Event Without Identified Device or Use Problem 22 Device
2022 Limb Fracture 4 Patient
2022 Positioning Problem 1 Device
2022 Migration 1 Device
2022 Break 9 Device
2022 Adverse Event Without Identified Device or Use Problem 27 Device
2021 Adverse Event Without Identified Device or Use Problem 1 Device
2019 Positioning Problem 1 Device
2019 Migration 3 Device
2019 Break 21 Device
2019 Adverse Event Without Identified Device or Use Problem 95 Device
2018 Migration 3 Device
2018 Improper or Incorrect Procedure or Method 1 Device
2018 Break 43 Device
2018 Adverse Event Without Identified Device or Use Problem 93 Device
2018 Activation, Positioning or Separation Problem 1 Device
2017 Unintended Movement 1 Device
2017 Malposition of Device 1 Device
2017 Difficult to Insert 1 Device
2017 Difficult To Position 1 Device
2017 Break 29 Device
2017 Adverse Event Without Identified Device or Use Problem 110 Device
2016 Unintended Movement 1 Device
2016 Inadequacy of Device Shape and/or Size 1 Device
2016 Improper or Incorrect Procedure or Method 1 Device
2016 Device Handling Problem 18 Device
2016 Break 40 Device
2016 Adverse Event Without Identified Device or Use Problem 55 Device
2015 Mechanics Altered 1 Device
2015 Loose or Intermittent Connection 1 Device
2015 Fracture 3 Device
2015 Fitting Problem 1 Device
2015 Failure to Align 1 Device
2015 Failure To Adhere Or Bond 2 Device
2015 Device Operates Differently Than Expected 1 Device
2015 Break 11 Device
2015 Appropriate Term/Code Not Available 1 Device
2015 Adverse Event Without Identified Device or Use Problem 2 Device
2014 Adverse Event Without Identified Device or Use Problem 1 Device
2013 Device Handling Problem 1 Device