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

A/K SOCKET

K Number: K802911 · Decision Dec 17, 1980
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
0
Applicant Total
16
Review Days
30

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
A/K SOCKET
K Number
K802911
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3420
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Orthomedics
Date Received
November 17, 1980
Decision Date
December 17, 1980
Product Code
ISS
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
ISS Prosthesis, Thigh Socket, External Component

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 →