510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
LHGClass II

Electrode, Spinal Epidural

21 CFR 882.5880 / Neurology
FDA source (opens on fda.gov)

LHG is the FDA product code for Electrode, Spinal Epidural, a class II device type, regulated under 21 CFR 882.5880. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LHG
Device name
Electrode, Spinal Epidural
Regulation
21 CFR 882.5880
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code LHG

By decision year
1 clearance under product code LHG with a decision year between 2011 and 2011, 2011 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LHG by decision year
YearClearances
20111

Applicants with the most clearances

Product code LHG
Applicants holding the most 510(k) clearances under product code LHG
ApplicantClearances
Abbott Medical1

Companies listing this code with FDA

Companies whose registered establishments list this code