Implants for surgery - Metallic materials - Part 6: Wrought
cobalt-nickel-chromium-molybdenum alloy
This National Standard of Canada is equivalent to International Standard ISO 5832-6:1997.
1 Scope
This part of ISO 5832 specifies the characteristics of, and corresponding test
methods for, wrought cobalt-nickel-chromium-molybdenum alloy for use in the
manufacture of surgical implants.
NOTE - The mechanical properties of a sample obtained from a finished product
made of this alloy…
This National Standard of Canada is equivalent to International Standard ISO 5833:1992.
1 Scope
This International Standard applies to radio-opaque and non-radio-opaque
cements and specifies physical, mechanical, packaging and labelling
requirements for self-curing resin cement based on poly(methacrylic acid
esters), of two types intended respectively for use with a syringe or in the…
Implants for surgery - Metal bone screws with hexagonal drive connection, spherical under-surface of...
This National Standard of Canada is equivalent to International Standard ISO 5835:1991.
1 Scope
This International Standard specifies dimensions and tolerances for metal bone
screws used in surgery, having hexagonal drive connection, spherical
under-surface of the head, and shallow and deep asymmetrical threads.
NOTEs
1 The mechanical requirements for screws that are cited in…
Implants for surgery - Partial and total hip joint prostheses - Part 2: Articulating surfaces made o...
This National Standard of Canada is equivalent to International Standard ISO 7206-2:1996.
1 Scope
This part of ISO 7206 specifies requirements for the articulating surfaces of
those types of total and partial hip joint prostheses that provide a joint
replacement of ball and socket configuration, as follows:
a) sphericity and surface finish requirements for metallic and ceramic…
Implants for surgery - Femoral and tibial components for partial and total knee joint prostheses - P...
This National Standard of Canada is equivalent to International Standard ISO 7207-1:1994.
1 Scope
This part of ISO 7207 classifies femoral and tibial components for knee joint
prostheses in which one or both bearing surfaces of at least one compartment of
the knee are replaced, and gives definitions of components and the designation
of dimensions.
Patellar components and prostheses…
Orthopaedic instruments - Drive connections - Part 1: Keys for use with screws with hexagon socket h...
This National Standard of Canada is equivalent to International Standard ISO 8319-1:1996.
1 Scope
This part of ISO 8319 specifies the dimensions, tolerances, mechanical
properties and performance requirements of the working end of keys to be used
for inserting and removing metal bone screws with hexagon drive sockets, used
as surgical implants.
Screw keys with a working end specified…
Orthopaedic instruments - Drive connections - Part 2: Screwdrivers for single slot head screws, scre...
This National Standard of Canada is equivalent to International Standard ISO 8319/2-1986.
1 Scope and field of application
This part of ISO 8319 specifies requirements for screwdrivers used in
orthopaedic surgery for inserting and removing bone screws with single slot
heads, with cruciate slot or cross-recessed heads.
Screwdrivers specified in this part of ISO 8319 are suitable for use…
Biological evaluation of medical devices - Part 9: Framework for identification
and quantification ...
This National Standard of Canada is equivalent to International Standard ISO 10993-9:1999.
1 Scope
This part of ISO 10993 provides general principles for the systematic
evaluation of the potential and observed biodegradation of medical devices and
for the design and performance of biodegradation studies.
This part of ISO 10993 is not applicable to:
a) viable-tissue engineered…
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation...
This National Standard of Canada is equivalent to International Standard ISO 10993-13:1998.
1 Scope
This part of ISO 10993 provides guidance on general requirements for the design
of tests for identifying and quantifying degradation products from finished
polymeric medical devices ready for clinical use.
This part of ISO 10993 describes two test methods to generate degradation…
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation produ...
This National Standard of Canada is equivalent to International Standard ISO 10993-16:1997.
1 Scope
This part of ISO 10993 gives principles on how toxicokinetic studies relevant
to medical devices should be designed and performed. Annex A describes the
considerations for inclusion of toxicokinetic studies in the biological
evaluation of medical devices.