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

NEOPRENE KNEE SUPPORT

K Number: K812423 · Decision Sep 14, 1981
Classifications
1
FEI Numbers
442
Registration Numbers
442
Same Product Code
14
Applicant Total
9
Review Days
21

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NEOPRENE KNEE SUPPORT
K Number
K812423
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Surgical Appliance Industries, Inc.
Date Received
August 24, 1981
Decision Date
September 14, 1981
Product Code
ITQ
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
ITQ Joint, Knee, External Brace

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ITQ), ordered by most recent decision date.

View all

Other Clearances by Surgical Appliance Industries, Inc.

K Number Device Name
K121106 TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR COMPRESSION GAUNTLET
K821682 TRUNCAL ORTHOSIS
K813416 EXTERNAL BREAST PROSTHESIS
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