510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K020480Substantially Equivalent

Rbm

Smith & Nephew, Inc., Mansfield MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K020480 is the FDA 510(k) clearance record for RBM, a class I device, cleared for Smith & Nephew, Inc. on under FDA product code KGS (Retention Device, Suture). FDA records list 572 510(k) clearances for Smith & Nephew, Inc., from to . As of , FDA records show one recall naming K020480.

Clearance record

Decision date
Received
(27 days to decision)
Product code
KGS Retention Device, Suture
Regulation
21 CFR 878.4930
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Smith & Nephew, Inc. 130 Forbes Blvd., Mansfield MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KGS

Trailing 12 months

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

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