Quick Links: Skip to main page content
Skip to Search
Skip to Topics Menu
Skip to Common Links
U.S. Food & Drug Administration
Follow FDA
En Español
Search FDA
Home
Food
Drugs
Medical Devices
Radiation-Emitting Products
Vaccines, Blood & Biologics
Animal & Veterinary
Cosmetics
Tobacco Products
TPLC - Total Product Life Cycle
FDA Home
medical devices
databases
-
510(k)
|
DeNovo
|
Registration & Listing
|
Adverse Events
|
Recalls
|
PMA
|
HDE
|
Classification
|
Standards
CFR Title 21
|
Radiation-Emitting Products
|
X-Ray Assembler
|
Medsun Reports
|
CLIA
|
TPLC
New Search
show TPLC since
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
Back to Search Results
Device
neurosurgical nerve locator
Definition
To locate or monitor function of spinal nerve roots or peripheral nerves during neurosurgery.
Product Code
PDQ
Regulation Number
874.1820
Device Class
2
Premarket Reviews
Manufacturer
Decision
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
-
-