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

HIP ABDUCTION SPLINT

K Number: K810557 · Decision Mar 13, 1981
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
3
Applicant Total
16
Review Days
11

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Basic Information

Device Name
HIP ABDUCTION SPLINT
K Number
K810557
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3665
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Orthomedics
Date Received
March 2, 1981
Decision Date
March 13, 1981
Product Code
IOZ
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
IOZ Splint, Abduction, Congenital Hip Dislocation

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
K810554 LUMBAR FLEXION BRACE
K810556 SPINAL EXTENSION BRACE
K803033 CRUSADER HYPEREXTENSION BRACE
Search all 16 clearances from Orthomedics →