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

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

Unknown
FDA source (opens on fda.gov)

LGW is the FDA product code for Stimulator, Spinal-Cord, Totally Implanted For Pain Relief, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 96 recalls.

Classification record

Product code
LGW
Device name
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
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
96

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 48 companies shown, in name order