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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device catheter, thrombus retriever
Regulation Description Percutaneous catheter.
Definition The device is intended to restore blood flow by removing thrombus/clots in patients experiencing ischemic stroke. The prior clearances in this category have been limited to simply identifying catheter placed in the peripheral, coronary, and neurovasculature. It is felt that this is a unique claim and should not be combined with previously cleared catheters under a general procode.
Product CodeNRY
Regulation Number 870.1250
Device Class 2


Premarket Reviews
ManufacturerDecision
ALEMBIC, LLC
  SUBSTANTIALLY EQUIVALENT 3
BALT USA, LLC
  SUBSTANTIALLY EQUIVALENT 1
CERENOVUS INC.
  SUBSTANTIALLY EQUIVALENT 1
CERENOVUS, INC.
  SUBSTANTIALLY EQUIVALENT 2
CODMAN & SHURTLEFF, INC.
  SUBSTANTIALLY EQUIVALENT 1
  1.  K193380  CERENOVUS Large Bore Catheter; CERENOVUS Aspiratio ...
IMPERATIVE CARE INC.
  SUBSTANTIALLY EQUIVALENT 3
IMPERATIVE CARE, INC.
  SUBSTANTIALLY EQUIVALENT 1
MICRO THERAPEUTICS INC. D/B/A EV3 NEUROVASCULAR
  SUBSTANTIALLY EQUIVALENT 1
MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR
  SUBSTANTIALLY EQUIVALENT 1
MICROVENTION INC.
  SUBSTANTIALLY EQUIVALENT 1
NEURAVI LTD.
  SUBSTANTIALLY EQUIVALENT 2
NEURAVI, LTD.
  SUBSTANTIALLY EQUIVALENT 1
PENUMBRA, INC.
  SUBSTANTIALLY EQUIVALENT 6
PERFUZE LTD.
  SUBSTANTIALLY EQUIVALENT 2
Q'APEL MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
RAPID MEDICAL LTD.
  SUBSTANTIALLY EQUIVALENT 3
ROUTE 92 MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 2
SCIENTIA VASCULAR INC
  SUBSTANTIALLY EQUIVALENT 1
WALLABY MEDICAL
  SUBSTANTIALLY EQUIVALENT 2

MDR Year MDR Reports MDR Events
2020 703 703
2021 688 688
2022 549 549
2023 711 711
2024 641 641
2025 68 68

Device Problems MDRs with this Device Problem Events in those MDRs
Adverse Event Without Identified Device or Use Problem 1553 1553
Break 564 564
Physical Resistance/Sticking 502 502
Fracture 295 295
Material Deformation 251 251
Stretched 164 164
Difficult to Remove 126 126
Failure to Advance 103 103
Material Separation 81 81
Retraction Problem 72 72
Material Twisted/Bent 60 60
Difficult to Advance 42 42
Crack 40 40
Suction Problem 40 40
Unraveled Material 35 35
Suction Failure 33 33
Fluid/Blood Leak 31 31
No Apparent Adverse Event 30 30
Detachment of Device or Device Component 29 29
Material Puncture/Hole 23 23
Leak/Splash 18 18
Separation Failure 16 16
Patient-Device Incompatibility 13 13
Entrapment of Device 12 12
Peeled/Delaminated 10 10
Packaging Problem 10 10
Material Split, Cut or Torn 9 9
Unclear Information 8 8
Use of Device Problem 8 8
Activation Failure 7 7
Premature Separation 7 7
Appropriate Term/Code Not Available 6 6
Device Fell 5 5
Material Frayed 5 5
Misconnection 5 5
Power Problem 5 5
Deformation Due to Compressive Stress 4 4
Device Handling Problem 4 4
Insufficient Information 4 4
Device Contamination with Body Fluid 4 4
Activation Problem 4 4
Activation, Positioning or Separation Problem 4 4
Component or Accessory Incompatibility 3 3
Decrease in Suction 3 3
Migration 3 3
Device Dislodged or Dislocated 3 3
Unintended Movement 3 3
Connection Problem 3 3
Component Missing 3 3
Lack of Effect 3 3

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 1249 1249
Intracranial Hemorrhage 652 652
No Consequences Or Impact To Patient 360 360
Thromboembolism 170 170
Hemorrhage/Bleeding 164 164
Vascular Dissection 156 156
Perforation of Vessels 146 146
Stroke/CVA 140 140
Ischemia Stroke 137 137
Vasoconstriction 134 134
Foreign Body In Patient 130 130
Insufficient Information 110 110
Embolism/Embolus 103 103
Obstruction/Occlusion 98 98
Unspecified Nervous System Problem 95 95
Hematoma 87 87
Swelling/ Edema 67 67
Thrombosis/Thrombus 66 66
Device Embedded In Tissue or Plaque 59 59
Death 56 56
Hemorrhagic Stroke 35 35
Cerebral Edema 32 32
Extravasation 32 32
Hemorrhage, Subarachnoid 30 30
No Known Impact Or Consequence To Patient 29 29
Stenosis 29 29
Ischemia 29 29
Rupture 28 28
Pseudoaneurysm 25 25
Fistula 24 24
Perforation 24 24
Infarction, Cerebral 22 22
Muscle Weakness 21 21
Paralysis 17 17
Dysphasia 17 17
Hemorrhage, Cerebral 16 16
Cognitive Changes 14 14
Respiratory Failure 12 12
Coma 12 12
Embolus 12 12
Paresis 11 11
No Code Available 11 11
Headache 11 11
Occlusion 10 10
Nervous System Injury 10 10
Hydrocephalus 10 10
Heart Failure/Congestive Heart Failure 10 10
Convulsion/Seizure 9 9
Aneurysm 8 8
Aspiration/Inhalation 8 8

Recalls
Manufacturer Recall Class Date Posted
1 IMPERATIVE CARE INC I Sep-29-2021
2 MICROVENTION INC. II Sep-17-2024
3 Penumbra Inc. I Jan-18-2021
4 ROUTE 92 MEDICAL INC I Apr-24-2024
5 Stryker Neurovascular II May-28-2024
6 Stryker Neurovascular II Mar-31-2020
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