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The commenter stated that the ReActiv8 ( has FDA approval [247] through the premarket process and is indicated for bilateral stimulation of the L2 medial branch of the dorsal ramus as it crosses the transverse process at L3 as an aid in the management of intractable chronic low back pain associated with multifidus muscle dysfunction, as evidenced by imaging or physiological testing in adults who have failed therapy including pain medications and physical therapy and are not candidates for spine surgery
Yartsev, Y
It has not been approved by MOHAP, DHA, DoH, FDA, or EMA to diagnose, treat, prevent, mitigate, or cure any condition
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