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TPLC
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Device
dura substitute
Regulation Description
Dura substitute.
Product Code
GXQ
Regulation Number
882.5910
Device Class
2
Premarket Reviews
Manufacturer
Decision
COLLAGEN MATRIX, INC.
SUBSTANTIALLY EQUIVALENT
1
HELIOS BIOMEDICAL, INC.
SUBSTANTIALLY EQUIVALENT
1
NURAMI MEDICAL , LTD.
SUBSTANTIALLY EQUIVALENT
1
SYNTHES (USA) PRODUCTS, LLC
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2021
76
76
2022
59
59
2023
109
110
2024
55
55
2025
63
63
2026
24
24
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
228
229
Insufficient Information
48
48
Material Puncture/Hole
17
17
Fluid/Blood Leak
13
13
Lack of Effect
12
12
Material Disintegration
9
9
Degraded
8
8
Patient Device Interaction Problem
8
8
Failure to Seal
7
7
Nonstandard Device
6
6
Break
5
5
Material Split, Cut or Torn
4
4
Material Separation
4
4
Material Integrity Problem
4
4
Material Rupture
3
3
Naturally Worn
2
2
Device Appears to Trigger Rejection
2
2
Appropriate Term/Code Not Available
2
2
Material Deformation
2
2
Adhesive Too Strong
2
2
Microbial Contamination of Device
2
2
Material Erosion
2
2
Device Contaminated During Manufacture or Shipping
2
2
Compatibility Problem
2
2
Difficult to Remove
1
1
Contamination /Decontamination Problem
1
1
Contamination
1
1
Loosening of Implant Not Related to Bone-Ingrowth
1
1
Therapeutic or Diagnostic Output Failure
1
1
Expiration Date Error
1
1
Material Perforation
1
1
Patient-Device Incompatibility
1
1
Delivered as Unsterile Product
1
1
Device Markings/Labelling Problem
1
1
Device Damaged Prior to Use
1
1
Misassembly by Users
1
1
Device Handling Problem
1
1
Product Quality Problem
1
1
Off-Label Use
1
1
No Apparent Adverse Event
1
1
Fracture
1
1
Device Dislodged or Dislocated
1
1
Mechanical Problem
1
1
Gel Leak
1
1
Expulsion
1
1
Calcified
1
1
Loose or Intermittent Connection
1
1
Fitting Problem
1
1
Biocompatibility
1
1
Leak/Splash
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Cerebrospinal Fluid Leakage
152
153
Unspecified Infection
42
42
Meningitis
37
38
Headache
31
31
No Clinical Signs, Symptoms or Conditions
21
21
Failure of Implant
20
20
Bacterial Infection
19
19
Insufficient Information
16
16
Post Operative Wound Infection
16
16
Swelling/ Edema
14
14
Fever
14
14
Hematoma
13
14
Hydrocephalus
12
13
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
11
11
Abscess
11
11
Hypersensitivity/Allergic reaction
10
10
Foreign Body Reaction
9
9
Cerebral Edema
8
8
Pain
8
8
Fistula
7
8
Hemorrhage/Bleeding
7
7
Unspecified Tissue Injury
7
8
Adhesion(s)
7
7
Fungal Infection
5
5
Cyst(s)
5
5
Inflammation
5
5
Purulent Discharge
5
5
Sepsis
4
4
Low Blood Pressure/ Hypotension
3
3
Cancer
3
3
Discomfort
3
3
Paralysis
3
3
Local Reaction
3
3
Impaired Healing
3
3
Fatigue
3
3
Emotional Changes
3
3
Implant Pain
2
2
Cramp(s) /Muscle Spasm(s)
2
2
Unspecified Nervous System Problem
2
2
Wound Dehiscence
2
2
Convulsion/Seizure
2
2
Speech Disorder
2
2
Nausea
2
2
Numbness
2
2
Anaphylactic Shock
2
2
Fluid Discharge
2
2
Bradycardia
2
2
Hearing Impairment
1
1
Ambulation Difficulties
1
1
High Blood Pressure/ Hypertension
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Collagen Matrix, Inc.
II
Feb-24-2022
2
Cook Biotech, Inc.
II
Jan-10-2025
3
Integra LifeSciences Corp.
II
Oct-30-2024
4
Medtronic Neurosurgery
II
Jul-20-2023
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