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TPLC
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show TPLC since
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Device
condylar plate fixation implant
Product Code
JDP
Regulation Number
888.3030
Device Class
2
Premarket Reviews
Manufacturer
Decision
DEPUY SYNTHES
SUBSTANTIALLY EQUIVALENT
1
SYNTHES USA
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2014
55
55
2015
97
97
2016
117
117
2017
46
46
2018
56
56
2019
49
49
2020
56
56
2021
79
79
2022
61
61
2023
29
29
2024
19
19
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
254
254
Adverse Event Without Identified Device or Use Problem
229
229
Device-Device Incompatibility
64
64
Unintended Movement
35
35
Migration or Expulsion of Device
15
15
Material Twisted/Bent
14
14
Bent
10
10
Material Deformation
9
9
Device Slipped
7
7
Migration
7
7
Detachment of Device or Device Component
7
7
Fitting Problem
6
6
Loose or Intermittent Connection
6
6
Failure To Adhere Or Bond
5
5
Insufficient Information
4
4
No Apparent Adverse Event
4
4
Crack
3
3
Use of Device Problem
3
3
Packaging Problem
3
3
Malposition of Device
2
2
Fracture
2
2
Device Dislodged or Dislocated
2
2
Appropriate Term/Code Not Available
2
2
Device Operates Differently Than Expected
2
2
Corroded
2
2
Material Integrity Problem
1
1
Component or Accessory Incompatibility
1
1
Operating System Becomes Nonfunctional
1
1
Loosening of Implant Not Related to Bone-Ingrowth
1
1
Mechanical Problem
1
1
Difficult To Position
1
1
Device Contamination with Chemical or Other Material
1
1
Failure to Capture
1
1
Device Inoperable
1
1
Mechanical Jam
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Non-union Bone Fracture
198
198
Failure of Implant
186
186
No Code Available
151
151
Pain
76
76
Unspecified Infection
64
64
No Clinical Signs, Symptoms or Conditions
55
55
Impaired Healing
54
54
Bone Fracture(s)
27
27
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
21
21
Fall
17
17
Insufficient Information
16
16
No Consequences Or Impact To Patient
12
12
Malunion of Bone
12
12
Discomfort
9
9
Reaction
9
9
No Known Impact Or Consequence To Patient
8
8
Burn(s)
8
8
Wound Dehiscence
6
6
Hip Fracture
6
6
Limited Mobility Of The Implanted Joint
6
6
Swelling
5
5
No Patient Involvement
5
5
Arthritis
4
4
Device Embedded In Tissue or Plaque
3
3
No Information
3
3
Unspecified Tissue Injury
3
3
Irritation
3
3
Injury
3
3
Sedation
3
3
Ambulation Difficulties
2
2
Physical Asymmetry
2
2
Swelling/ Edema
2
2
Calcium Deposits/Calcification
2
2
Osteolysis
2
2
Loss of Range of Motion
2
2
Thrombosis/Thrombus
2
2
Not Applicable
2
2
Joint Dislocation
2
2
Death
2
2
Nerve Damage
1
1
Limb Fracture
1
1
Post Operative Wound Infection
1
1
Local Reaction
1
1
Dysphagia/ Odynophagia
1
1
Ischemia
1
1
Inflammation
1
1
Deformity/ Disfigurement
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Synthes USA HQ, Inc.
II
Nov-26-2013
2
Synthes, Inc.
II
Mar-04-2014
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