Code of Federal Regulations 21 Parts 800 to 1299 Food and Drugs: Revised as of April 1 2006U.S. Government Printing Office, 2006 - 796 lappuses The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This volumwe contains the regulations about medical devices. |
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480. lappuse
... joint metal / composite semi- constrained cemented prosthesis . 888.3110 Ankle joint metal / polymer semi- constrained cemented prosthesis . 888.3120 Ankle joint metal / polymer non - con- strained cemented prosthesis . 888.3150 Elbow ...
... joint metal / composite semi- constrained cemented prosthesis . 888.3110 Ankle joint metal / polymer semi- constrained cemented prosthesis . 888.3120 Ankle joint metal / polymer non - con- strained cemented prosthesis . 888.3150 Elbow ...
490. lappuse
... joint polymer con- strained prosthesis . ( a ) Identification . A finger joint poly- mer constrained prosthesis is a device intended to be implanted to replace a metacarpophalangeal or proximal interphalangeal ( finger ) joint . This ge ...
... joint polymer con- strained prosthesis . ( a ) Identification . A finger joint poly- mer constrained prosthesis is a device intended to be implanted to replace a metacarpophalangeal or proximal interphalangeal ( finger ) joint . This ge ...
501. lappuse
... Joint Metal / Polymer / Metal Nonconstrained Semi - Constrained Uncemented Prosthesis . " or Porous - Coated [ 66 FR 12737 , Feb. 28 , 2001 ] joint § 888.3680 Shoulder glenoid ( hemi - shoulder ) metallic cemented prosthesis . ( a ) ...
... Joint Metal / Polymer / Metal Nonconstrained Semi - Constrained Uncemented Prosthesis . " or Porous - Coated [ 66 FR 12737 , Feb. 28 , 2001 ] joint § 888.3680 Shoulder glenoid ( hemi - shoulder ) metallic cemented prosthesis . ( a ) ...
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AC-powered accessories accreditation body amended at 65 ance standards application blood cardiopulmonary bypass catheter chapter subject Class II perform Class II special Classification clinical clude commercial distribution complaint files component current good manufacturing Date PMA dental denture device intended device is exempt device that consists disease electronic equipment facility FDA's fluoroscopic Food and Drug guidance document Identification image receptor immunological test system implanted intended for medical intended to measure July 25 labeling limitations mammography manufacturing practice manufacturing practice regula means medical purposes ment monitor notice of completion paragraph patient PDP is required plasma PMA or notice postmarket surveillance premarket approval premarket notification procedures procedures in subpart prosthesis radiation reagents regulation requirements concerning records respect to complaint Sept serological serum special controls specific submit subpart E surgical tion tissue trols type of device vice x-ray system