FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TRUNCAL ORTHOSIS

K Number: K821682 · Decision Jun 24, 1982
Classifications
1
FEI Numbers
323
Registration Numbers
323
Same Product Code
3
Applicant Total
9
Review Days
16

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Basic Information

Device Name
TRUNCAL ORTHOSIS
K Number
K821682
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3490
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Surgical Appliance Industries, Inc.
Date Received
June 8, 1982
Decision Date
June 24, 1982
Product Code
IQE
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IQE Orthosis, Lumbar

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K Number Device Name
K121106 TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR COMPRESSION GAUNTLET
K813416 EXTERNAL BREAST PROSTHESIS
K812423 NEOPRENE KNEE SUPPORT
K812401 CRUCIFORM ANTERIOR SPINAL HYPEREXTEN. O
K812422 CUSTOM CONTOUR LUMBOSACRAL ORTHOSIS
K811689 CYLINDER KNEE CAST/SPLINT
K811690 ANKLE-FOOT CAST/SPLINT
K811494 LUMBO-SACRAL FLEXION ORTHOSIS