[Code of Federal Regulations]
[Title 21, Volume 8]
[Revised as of April 1, 2002]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR890.3420]

[Page 491]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 890--PHYSICAL MEDICINE DEVICES--Table of Contents
 
             Subpart D--Physical Medicine Prosthetic Devices
 
Sec. 890.3420  External limb prosthetic component.

    (a) Identification. An external limb prosthetic component is a 
device intended for medical purposes that, when put together with other 
appropriate components, constitutes a total prosthesis. Examples of 
external limb prosthetic components include the following: Ankle, foot, 
hip, knee, and socket components; mechanical or powered hand, hook, 
wrist unit, elbow joint, and shoulder joint components; and cable and 
prosthesis suction valves.
    (b) Classification. Class I (general controls). The device is exempt 
from the premarket notification procedures in subpart E of part 807 of 
this chapter, subject to the limitations in Sec. 890.9. The device is 
also exempt from the current good manufacturing practice regulations in 
part 820 of this chapter, with the exception of Sec. 820.180, regarding 
general requirements concerning records and Sec. 820.198, regarding 
complaint files.

[48 FR 53047, Nov. 23, 1983, as amended at 66 FR 38816, July 25, 2001]