Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

New Search show TPLC since Back to Search Results
Device prosthesis, wrist, 2 part metal-plastic articulation, semi-constrained
Product CodeJWI
Regulation Number 888.3800
Device Class 2

MDR Year MDR Reports MDR Events
2018 1 1
2019 2 2
2022 1 1
2023 2 2
2024 5 5

Device Problems MDRs with this Device Problem Events in those MDRs
Naturally Worn 5 5
Device Dislodged or Dislocated 2 2
Material Discolored 1 1
Adverse Event Without Identified Device or Use Problem 1 1
Fracture 1 1
Protective Measures Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Pain 5 5
Swelling/ Edema 4 4
Loss of Range of Motion 3 3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Joint Dislocation 2 2
Patient Problem/Medical Problem 1 1
Unspecified Infection 1 1
Hypersensitivity/Allergic reaction 1 1
No Clinical Signs, Symptoms or Conditions 1 1
Emotional Changes 1 1
Synovitis 1 1
Rupture 1 1
Foreign Body Reaction 1 1
Bone Shedding Debris 1 1
Insufficient Information 1 1
Osteolysis 1 1

-
-