510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K180949Substantially Equivalent

Steribite

Rjr Surgical, Inc., Cleveland OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K180949 is the FDA 510(k) clearance record for Steribite, a class II device, cleared for Rjr Surgical, Inc. on under FDA product code HAE (Rongeur, Manual). FDA records list one 510(k) clearance for Rjr Surgical, Inc. As of , FDA records show no recalls naming K180949.

Clearance record

Decision date
Received
(211 days to decision)
Product code
HAE Rongeur, Manual
Regulation
21 CFR 882.4840
Device class
Class II
Review panel
Neurology
Applicant
Rjr Surgical, Inc. 2530 Superior Ave., Cleveland OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HAE

Trailing 12 months
1 clearance under product code HAE in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HAE, 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 20261
October 20260