510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K222281Substantially Equivalent

Intracept Intraosseous Nerve Ablation System

Relievant Medsystems, Sunnyvale CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222281 is the FDA 510(k) clearance record for Intracept Intraosseous Nerve Ablation System, a class II device, cleared for Relievant Medsystems, Inc. on under FDA product code GXI (Probe, Radiofrequency Lesion). FDA records list 10 510(k) clearances for Relievant Medsystems, Inc., from to . As of , FDA records show one recall naming K222281.

Clearance record

Decision date
Received
(89 days to decision)
Product code
GXI Probe, Radiofrequency Lesion
Regulation
21 CFR 882.4725
Device class
Class II
Review panel
Neurology
Applicant
Relievant Medsystems, Inc. 1230 Midas Way, Sunnyvale CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GXI

Trailing 12 months
2 clearances under product code GXI in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GXI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260