510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K790307Substantially Equivalent

Flexible Reamer, Guide Wire System

3M Company, White City OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K790307 is the FDA 510(k) clearance record for FLEXIBLE REAMER, GUIDE WIRE SYSTEM, a class I device, cleared for 3M Company on under FDA product code HTO (Reamer). FDA records list 54 510(k) clearances for 3M Company, from to . As of , FDA records show no recalls naming K790307.

Clearance record

Decision date
Received
(9 days to decision)
Product code
HTO Reamer
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Applicant
3M Company 8124 Pacific Ave., White City OR
Third party review
No

Clearances, product code HTO

Trailing 12 months

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

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