DEVICE: Actua Knee Hydraulic (00850013242320)
Device Identifier (DI) Information
Actua Knee Hydraulic
CA603-PHY
In Commercial Distribution
CA603-PHY
CYPRESS ADAPTIVE, LLC
CA603-PHY
In Commercial Distribution
CA603-PHY
CYPRESS ADAPTIVE, LLC
The Actua Knee Hydraulic is a polycentric hydraulic knee joint with stance flexion feature and interchangeable spring extension assist. The stance flexion can be tuned infinitely, which ensures optimal comfort during loading response. The patented horizontal hydraulic cylinder contributes to the compact size of this hydraulic knee joint. In addition, maintenance is easy with the innovative oil-refill system.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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43795 | Polycentric mechanical knee prosthesis |
An artificial substitute for a transfemoral (above-the-knee) and/or knee disarticulation amputation designed as a component of an external lower-limb prosthesis to restore some of the appearance and/or function of the normal anatomy. It typically consists of metal and plastic and is constructed as a multiple-axis joint rotation, mechanical hinge that incorporates friction adjustment and a simple swing control that permits variable walking speed. A common design, known as a “fourbar” knee, is very stable during early stance phase (beginning of a step), reduces the leg’s length when beginning a step lowering the risk of stumbling, and bends in the swing phase or when the user sits down.
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Obsolete | false |
FDA Product Code
[?]Product Code | Product Code Name |
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ISY | Joint, Knee, External Limb Component |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
98dd1145-7410-4585-bb6a-94db41cd8250
December 10, 2019
1
December 02, 2019
December 10, 2019
1
December 02, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
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Secondary DI
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Unit of Use DI
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Unit of Use DI Number:
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Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
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No Customer Contact currently defined