510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K011676Substantially Equivalent

Vivawave Microwave System

Vivant Medical, Inc., Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K011676 is the FDA 510(k) clearance record for VIVAWAVE MICROWAVE SYSTEM, a class II device, cleared for Vivant Medical, Inc. on under FDA product code NEY (System, Ablation, Microwave And Accessories). FDA records list 10 510(k) clearances for Vivant Medical, Inc., from to . As of , FDA records show one recall naming K011676.

Clearance record

Decision date
Received
(384 days to decision)
Product code
NEY System, Ablation, Microwave And Accessories
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Vivant Medical, Inc. 1916-A Old Middlefield Way, Mountain View CA
510(k) summary
Summary
Third party review
No

Clearances, product code NEY

Trailing 12 months
2 clearances under product code NEY in the twelve months to October 2026, March 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code NEY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20262
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260