510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K994262Substantially Equivalent

Frontal Sinus Trephination Cannula

Xomed, Inc., Jacksonville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K994262 is the FDA 510(k) clearance record for FRONTAL SINUS TREPHINATION CANNULA, a class I device, cleared for Xomed, Inc. on under FDA product code KAM (Cannula, Sinus). FDA records list 46 510(k) clearances for Xomed, Inc., from to . As of , FDA records show no recalls naming K994262.

Clearance record

Decision date
Received
(53 days to decision)
Product code
KAM Cannula, Sinus
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Xomed, Inc. 6743 Southpoint Dr. N., Jacksonville FL
510(k) summary
Summary
Third party review
No

Clearances, product code KAM

Trailing 12 months

FDA records hold no clearances under product code KAM in the trailing twelve months.

FDA records show no clearances under product code KAM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KAM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260