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Subpart B—Cardiovascular Diagnostic Devices
CFR Sub-Part
Subpart B—Diagnostic Devices
CFR Sub-Part
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
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
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
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 16 August 2024 at 11:05 pm
NE
/
subpart-e—surgical-devices
/
HST
/
K862874
View Source
THE TOWERED 90/90 UNIT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862874
510(k) Type
Traditional
Applicant
LOSSING ORTHOPEDIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1986
Days to Decision
8 days
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
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
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
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-e—surgical-devices
/
HST
/
K862874
View Source
THE TOWERED 90/90 UNIT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862874
510(k) Type
Traditional
Applicant
LOSSING ORTHOPEDIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1986
Days to Decision
8 days