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Subpart B—Cardiovascular Diagnostic Devices
CFR Sub-Part
Subpart B—Diagnostic Devices
CFR Sub-Part
PDQ
Neurosurgical Nerve Locator
2
Product Code
K
22
3438
TELIGEN System Peripheral Motor Nerve Stimulation Indications
2
Cleared 510(K)
K
22
1821
ATEC IOM Accessory Instruments
2
Cleared 510(K)
K
22
0160
PediGuard Threaded
2
Cleared 510(K)
K
20
3684
Neurosign V4 Intraoperative Nerve Monitor
2
Cleared 510(K)
K
20
1454
DSG Connect Technology
2
Cleared 510(K)
K
19
1723
ATEC IOM Accessory Instruments
2
Cleared 510(K)
K
19
0163
ALARA Neuro Access Kit
2
Cleared 510(K)
K
18
2617
ATEC IOM Accessory Instruments
2
Cleared 510(K)
K
18
2662
NAV PAK Needle, NIM NAV PAK Needle
2
Cleared 510(K)
K
18
1559
Neurosign V4 Intraoperative Nerve Monitor
2
Cleared 510(K)
Show All 33 Submissions
HRW
Dynamometer, Nonpowered
1
Product Code
KQW
Goniometer, Nonpowered
1
Product Code
KQX
Goniometer, Ac-Powered
1
Product Code
LBB
Dynamometer, Ac-Powered
2
Product Code
NKI
Goniometer With Electrodes
2
Product Code
QWP
Optical Neurosurgical Nerve Locator
2
Product Code
Subpart B—Neurological Diagnostic Devices
CFR Sub-Part
Subpart B—Physical Medicine Diagnostic Devices
CFR Sub-Part
Subpart C—Cardiovascular Monitoring Devices
CFR Sub-Part
Subpart D—Physical Medicine Prosthetic Devices
CFR Sub-Part
Subpart E—Neurological Surgical Devices
CFR Sub-Part
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—Cardiovascular Therapeutic Devices
CFR Sub-Part
Subpart F—Neurological Therapeutic Devices
CFR Sub-Part
Subpart F—Physical Medicine Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
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Radiology
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General and Plastic Surgery
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Review Panel
Medical Genetics
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Unknown
Review Panel
Last synced on 20 December 2024 at 11:05 pm
NE
/
subpart-b—diagnostic-devices
/
PDQ
/
K201454
View Source
DSG Connect Technology
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201454
510(k) Type
Traditional
Applicant
SpineGuard, S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/10/2021
Days to Decision
254 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Miscellaneous
Subpart B—Cardiovascular Diagnostic Devices
Subpart B—Diagnostic Devices
PDQ
Neurosurgical Nerve Locator
K
22
3438
TELIGEN System Peripheral Motor Nerve Stimulation Indications
K
22
1821
ATEC IOM Accessory Instruments
K
22
0160
PediGuard Threaded
K
20
3684
Neurosign V4 Intraoperative Nerve Monitor
K
20
1454
DSG Connect Technology
K
19
1723
ATEC IOM Accessory Instruments
K
19
0163
ALARA Neuro Access Kit
K
18
2617
ATEC IOM Accessory Instruments
K
18
2662
NAV PAK Needle, NIM NAV PAK Needle
K
18
1559
Neurosign V4 Intraoperative Nerve Monitor
Show All 33 Submissions
HRW
Dynamometer, Nonpowered
KQW
Goniometer, Nonpowered
KQX
Goniometer, Ac-Powered
LBB
Dynamometer, Ac-Powered
NKI
Goniometer With Electrodes
QWP
Optical Neurosurgical Nerve Locator
Subpart B—Neurological Diagnostic Devices
Subpart B—Physical Medicine Diagnostic Devices
Subpart C—Cardiovascular Monitoring Devices
Subpart D—Physical Medicine Prosthetic Devices
Subpart E—Neurological Surgical Devices
Subpart E—Surgical Devices
Subpart F—Cardiovascular Therapeutic Devices
Subpart F—Neurological Therapeutic Devices
Subpart F—Physical Medicine Therapeutic Devices
Subpart F—Therapeutic Devices
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
NE
/
subpart-b—diagnostic-devices
/
PDQ
/
K201454
View Source
DSG Connect Technology
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201454
510(k) Type
Traditional
Applicant
SpineGuard, S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/10/2021
Days to Decision
254 days
Submission Type
Summary