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Wearable Vibration Device For Orthopedic Use

Page Type
Product Code
Definition
A wearable vibration device for orthopedic use is a wearable device that uses mechanical vibrations, targeted to specific regions of the skeleton, to reduce loss of bone strength or bone mineral density.
Physical State
Vibrator hardware. The device may include a motor, pressure sensor, and accelerometers within a casing, seated on a belt. The device may include software to regulate the magnitude of vibration generated and to control treatment duration.
Technical Method
Consists of a vibration pack which incorporates a motor that is designed to transmit low-amplitude, high-frequency vibration to the skeleton.
Target Area
Skeleton, excluding the skull and face.
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.5895
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZO is linked to regulation 21CFR888.5895, which does not seem to exist yet. It may be pending at the moment.

Wearable Vibration Device For Orthopedic Use

Page Type
Product Code
Definition
A wearable vibration device for orthopedic use is a wearable device that uses mechanical vibrations, targeted to specific regions of the skeleton, to reduce loss of bone strength or bone mineral density.
Physical State
Vibrator hardware. The device may include a motor, pressure sensor, and accelerometers within a casing, seated on a belt. The device may include software to regulate the magnitude of vibration generated and to control treatment duration.
Technical Method
Consists of a vibration pack which incorporates a motor that is designed to transmit low-amplitude, high-frequency vibration to the skeleton.
Target Area
Skeleton, excluding the skull and face.
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.5895
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZO is linked to regulation 21CFR888.5895, which does not seem to exist yet. It may be pending at the moment.