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FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
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Review Panel
Dental
Review Panel
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Review Panel
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Review Panel
General Hospital
Review Panel
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Review Panel
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Review Panel
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Review Panel
Cardiovascular Diagnostic Devices
CFR Sub-Part
Cardiovascular Monitoring Devices
CFR Sub-Part
Cardiovascular Therapeutic Devices
CFR Sub-Part
Diagnostic Devices
CFR Sub-Part
Miscellaneous
Miscellaneous
Neurological Diagnostic Devices
CFR Sub-Part
Neurological Surgical Devices
CFR Sub-Part
Neurological Therapeutic Devices
CFR Sub-Part
Physical Medicine Diagnostic Devices
CFR Sub-Part
Physical Medicine Prosthetic Devices
CFR Sub-Part
Physical Medicine Therapeutic Devices
CFR Sub-Part
Surgical Devices
CFR Sub-Part
QQO
Cranial Measurement Software
1
Product Code
HST
Apparatus, Traction, Non-Powered
1
Product Code
K
16
2702
Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table
1
Cleared 510(K)
K
11
0858
LO-BAK TRAX
1
Cleared 510(K)
K
98
4190
BACK-ON-TRAC, MODEL 101BOT
1
Cleared 510(K)
K
87
2121
K AND D HOME TRACT
1
Cleared 510(K)
K
87
0212
ARTHROSCOPIC SHOULDER HOLDER
1
Cleared 510(K)
K
87
0125
EXTREMITY ELEVATOR
1
Cleared 510(K)
K
87
0102
TUPPER TROLLEY
1
Cleared 510(K)
K
86
4765
MODEL 668, TRACTION SPLINT, ADULT
1
Cleared 510(K)
K
86
2874
THE TOWERED 90/90 UNIT
1
Cleared 510(K)
K
86
0037
SUSPENDER ORTHOPEDIC SUSPENSION DEVICE
1
Cleared 510(K)
Show All 38 Submissions
ONO
Neurosurgical Laser With Mr Thermography
2
Product Code
Therapeutic Devices
CFR Sub-Part
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 26 May 2023 at 11:04 pm
NE
/
surgical-devices
/
HST
/
K870212
View Source
ARTHROSCOPIC SHOULDER HOLDER
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870212
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1987
Days to Decision
31 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Cardiovascular Diagnostic Devices
Cardiovascular Monitoring Devices
Cardiovascular Therapeutic Devices
Diagnostic Devices
Miscellaneous
Neurological Diagnostic Devices
Neurological Surgical Devices
Neurological Therapeutic Devices
Physical Medicine Diagnostic Devices
Physical Medicine Prosthetic Devices
Physical Medicine Therapeutic Devices
Surgical Devices
QQO
Cranial Measurement Software
HST
Apparatus, Traction, Non-Powered
K
16
2702
Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table
K
11
0858
LO-BAK TRAX
K
98
4190
BACK-ON-TRAC, MODEL 101BOT
K
87
2121
K AND D HOME TRACT
K
87
0212
ARTHROSCOPIC SHOULDER HOLDER
K
87
0125
EXTREMITY ELEVATOR
K
87
0102
TUPPER TROLLEY
K
86
4765
MODEL 668, TRACTION SPLINT, ADULT
K
86
2874
THE TOWERED 90/90 UNIT
K
86
0037
SUSPENDER ORTHOPEDIC SUSPENSION DEVICE
Show All 38 Submissions
ONO
Neurosurgical Laser With Mr Thermography
Therapeutic Devices
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
NE
/
surgical-devices
/
HST
/
K870212
View Source
ARTHROSCOPIC SHOULDER HOLDER
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870212
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1987
Days to Decision
31 days