Please ensure that the qualified personnel applying the product is not only authorised for fitting this knee joint, but
also for the connection to the osseointegrated implant system.
3 Application
3.1 Indications for use
The product is to be used solely for lower limb prosthetic fittings.
3.2 Conditions of use
The product was developed for everyday use and should not be used for walking speeds over 3 km/h or unusual
activities. These unusual activities include, for example, extreme sports (free climbing, parachuting, paragliding,
etc.).
Permissible ambient conditions are described in the technical data (see Page 34).
The prosthesis is intended for use exclusively on the patient for whom the adjustment was made. The manufac
turer does not authorise use of the prosthesis on another person.
Our components perform optimally when paired with appropriate components based upon weight and mobility
grades identifiable by our MOBIS classification information and which have appropriate modular connectors.
Activity mode A (locked mode)
This product is recommended for mobility grade 1 (indoor walker). Approved for a body weight of
max. 125kg.
m°
kg
Activity mode B (semi-locked mode)
This product is recommended for mobility grade 1 (indoor walker) and mobility grade 2 (restric
ted outdoor walker). Approved for a body weight of max. 125 kg.
m°
kg
Activity mode C (yielding mode)
This product is recommended for mobility grade 2 (restricted outdoor walker). Approved for a
body weight of max. 125 kg.
m°
kg
3.3 Indications
•
For patients with knee disarticulation or transfemoral amputation
•
For unilateral or bilateral amputation
•
Dysmelia patients with residual limb characteristics corresponding to knee disarticulation or a transfemoral
amputation
•
The patient must fulfil the physical and mental requirements for perceiving visual/acoustic signals and/or mech
anical vibrations.
3.4 Qualification
The product may be fitted only by qualified personnel authorised by Ottobock after completing the corresponding
training.
If the product is to be connected to an osseointegrated implant system, the qualified personnel must also be
authorised for the connection to the osseointegrated implant system.
Kenevo 3C60/3C60=ST
Application
9