Device classification

Stimulator, Osteogenesis, Electric, Battery-Operated, Invasive

Unknown

Class IIIProduct code HTM
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Third party flag
N
Life sustain support flag
N
Gmp exempt flag
N
Summary malfunction reporting
Eligible
Product code
HTM
Review panel
OR
Device name
Stimulator, Osteogenesis, Electric, Battery-Operated, Invasive
Medical specialty description
Unknown
Device class
3
Implant flag
N
Submission type ID
2
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.