510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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SGSClass III

Deep Brain Stimulation For The Treatment Of Dystonia

Unknown
FDA source (opens on fda.gov)

SGS is the FDA product code for Deep Brain Stimulation For The Treatment Of Dystonia, a class III device type. FDA's definition for this code reads: "To stimulate deep brain structure to manage dystonia symptoms". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
SGS
Device name
Deep Brain Stimulation For The Treatment Of Dystonia
FDA definition
To stimulate deep brain structure to manage dystonia symptoms
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code