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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device prosthesis, elbow, semi-constrained, cemented
Product CodeJDB
Regulation Number 888.3160
Device Class 2


Premarket Reviews
ManufacturerDecision
LIMACORPORATE S.P.A.
  SUBSTANTIALLY EQUIVALENT 1
TORNIER INC.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2019 30 30
2020 32 32
2021 23 23
2022 60 83
2023 30 30
2024 163 163

Device Problems MDRs with this Device Problem Events in those MDRs
Adverse Event Without Identified Device or Use Problem 136 141
Osseointegration Problem 54 62
Loosening of Implant Not Related to Bone-Ingrowth 38 38
Unstable 32 41
Fracture 22 22
Device Dislodged or Dislocated 20 38
Break 17 17
Insufficient Information 13 13
Loss of Osseointegration 12 12
Patient Device Interaction Problem 7 7
Naturally Worn 7 7
Appropriate Term/Code Not Available 6 6
Use of Device Problem 4 4
Detachment of Device or Device Component 4 4
Migration 4 4
Unintended Movement 3 3
Loss of or Failure to Bond 3 3
Migration or Expulsion of Device 2 2
Malposition of Device 2 2
Inaccurate Information 2 2
Device Slipped 1 1
Mechanical Problem 1 1
Material Erosion 1 1
Material Integrity Problem 1 1
Therapeutic or Diagnostic Output Failure 1 1
Degraded 1 1
Improper or Incorrect Procedure or Method 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Unspecified Infection 68 72
Inadequate Osseointegration 55 63
Joint Laxity 46 55
Bone Fracture(s) 37 37
Failure of Implant 35 35
Implant Pain 33 33
Insufficient Information 28 46
Loss of Range of Motion 22 22
Pain 20 20
No Information 15 15
Joint Dislocation 10 10
Osteolysis 10 10
No Code Available 9 9
No Clinical Signs, Symptoms or Conditions 9 9
Swelling/ Edema 9 9
Discomfort 9 9
Injury 7 7
Fall 5 5
Inadequate Pain Relief 4 4
Bacterial Infection 4 4
Fluid Discharge 4 4
No Known Impact Or Consequence To Patient 4 4
Ossification 4 4
Post Operative Wound Infection 4 4
Tissue Damage 3 3
Fever 3 3
Inflammation 3 3
Skin Inflammation/ Irritation 3 3
Sepsis 3 3
Foreign Body In Patient 2 2
Post Traumatic Wound Infection 2 2
Cyst(s) 2 2
Reaction 2 2
Limb Fracture 2 2
No Consequences Or Impact To Patient 2 2
Neuropathy 2 2
Foreign Body Reaction 1 1
Scar Tissue 1 1
Adhesion(s) 1 1
Rheumatoid Arthritis 1 1
Unspecified Tissue Injury 1 1
Wound Dehiscence 1 1
Erosion 1 1
Impaired Healing 1 1
Device Embedded In Tissue or Plaque 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Limacorporate S.p.A II Dec-20-2024
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