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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device neurosurgical nerve locator
Definition To locate or monitor function of spinal nerve roots or peripheral nerves during neurosurgery.
Product CodePDQ
Regulation Number 874.1820
Device Class 2


Premarket Reviews
ManufacturerDecision
ALPHATEC SPINE, INC
  SUBSTANTIALLY EQUIVALENT 1
ALPHATEC SPINE, INC.
  SUBSTANTIALLY EQUIVALENT 2
BOSTON ENDO SURGICAL TECH,
  SUBSTANTIALLY EQUIVALENT 2
MAGSTIM COMPANY LTD.
  SUBSTANTIALLY EQUIVALENT 2
MEDOS INTERNATIONAL SARL
  SUBSTANTIALLY EQUIVALENT 1
MEDOS INTERNATIONAL, SARL
  SUBSTANTIALLY EQUIVALENT 2
SPINE GUARD S.A.
  SUBSTANTIALLY EQUIVALENT 1
SPINEGUARD, S.A.
  SUBSTANTIALLY EQUIVALENT 1
SURGENTEC, LLC
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2018 5 5
2019 9 9
2020 9 9
2021 10 10
2022 16 16
2023 9 9

Device Problems MDRs with this Device Problem Events in those MDRs
Incorrect, Inadequate or Imprecise Result or Readings 9 9
Break 7 7
Adverse Event Without Identified Device or Use Problem 7 7
Device Alarm System 5 5
Fracture 5 5
Failure to Read Input Signal 4 4
Failure to Deliver Shock/Stimulation 3 3
Crack 2 2
Deflation Problem 2 2
Display or Visual Feedback Problem 2 2
Difficult to Remove 2 2
Inappropriate/Inadequate Shock/Stimulation 2 2
Patient-Device Incompatibility 2 2
Communication or Transmission Problem 1 1
Detachment of Device or Device Component 1 1
Material Twisted/Bent 1 1
Electromagnetic Interference 1 1
Entrapment of Device 1 1
False Negative Result 1 1
No Audible Alarm 1 1
Circuit Failure 1 1
Use of Device Problem 1 1
Device Damaged Prior to Use 1 1
Power Problem 1 1
Insufficient Information 1 1
Appropriate Term/Code Not Available 1 1
Patient Device Interaction Problem 1 1
Audible Prompt/Feedback Problem 1 1
Erratic Results 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 21 21
No Consequences Or Impact To Patient 6 6
Insufficient Information 4 4
Nerve Proximity Nos (Not Otherwise Specified) 4 4
Foreign Body In Patient 4 4
Paralysis 3 3
No Known Impact Or Consequence To Patient 3 3
Full thickness (Third Degree) Burn 2 2
Device Embedded In Tissue or Plaque 2 2
Burn, Thermal 2 2
Nerve Damage 2 2
Pain 2 2
No Code Available 1 1
Convulsion/Seizure 1 1
Dysgeusia 1 1
Injury 1 1
Hypoesthesia, Foot/Leg 1 1
Extubate 1 1
Numbness 1 1
Spinal Cord Injury 1 1
Anaphylactic Shock 1 1
Awareness during Anaesthesia 1 1
Edema 1 1
Muscle Spasm(s) 1 1
Nervous System Injury 1 1

Recalls
Manufacturer Recall Class Date Posted
1 NuVasive Inc II Jul-22-2020
2 The Magstim Company Limited II Aug-25-2020
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