510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K942748Substantially Equivalent for Some Indications

Intrasite

Smith & Nephew United, Inc., Largo FL / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K942748 is the FDA 510(k) clearance record for INTRASITE, a class I device, cleared for Smith & Nephew United, Inc. on under FDA product code NAE (Dressing, Wound, Hydrogel Without Drug And/Or Biologic). FDA records list 34 510(k) clearances for Smith & Nephew United, Inc., from to . As of , FDA records show no recalls naming K942748.

Clearance record

Decision date
Received
(19 days to decision)
Product code
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic
Regulation
21 CFR 878.4022
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Smith & Nephew United, Inc. 11775 Starkley Rd., Largo FL
Third party review
No

Clearances, product code NAE

Trailing 12 months

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

FDA records show no clearances under product code NAE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NAE, 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