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

HUMERAL FRACTURE BRACE

K Number: K802909 · Decision Dec 17, 1980
Classifications
1
FEI Numbers
503
Registration Numbers
503
Same Product Code
51
Applicant Total
16
Review Days
30

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Basic Information

Device Name
HUMERAL FRACTURE BRACE
K Number
K802909
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Orthomedics
Date Received
November 17, 1980
Decision Date
December 17, 1980
Product Code
IQI
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
IQI Orthosis, Limb Brace

Similar 510(k) Clearances

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Other Clearances by Orthomedics

K Number Device Name
K832740 FEMORAL FRACTURE ORTHOSIS
K832742 EXTENSION CONTROL KNEE ORTHOSIS
K832741 JASON CERVICAL ORTHOSIS
K811456 ORTHO-FRAC KIT
K811298 EXECUTIVE COLLAR
K811297 CERVICAL SUPPORT
K810555 SCOLIOSIS ORTHOTIC SYSTEM
K810557 HIP ABDUCTION SPLINT
K810554 LUMBAR FLEXION BRACE
K810556 SPINAL EXTENSION BRACE
Search all 16 clearances from Orthomedics →