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

Dorsal Root Ganglion Stimulator For Pain Relief

Unknown
FDA source (opens on fda.gov)

PMP is the FDA product code for Dorsal Root Ganglion Stimulator For Pain Relief, a class III device type. FDA's definition for this code reads: "Stimulation of the dorsal root ganglion for the treatment of chronic, intractable pain of the lower limbs". As of , FDA records hold no 510(k) clearances under this code and 2 recalls.

Classification record

Product code
PMP
Device name
Dorsal Root Ganglion Stimulator For Pain Relief
FDA definition
Stimulation of the dorsal root ganglion for the treatment of chronic, intractable pain of the lower limbs.
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
2

Companies listing this code with FDA

Companies whose registered establishments list this code