510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K840566Substantially Equivalent

Bone Stapling Fixation Sys

3M Company, St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840566 is the FDA 510(k) clearance record for BONE STAPLING FIXATION SYS, a class II device, cleared for 3M Company on under FDA product code JDR (Staple, Fixation, Bone). FDA records list 146 510(k) clearances for 3M Company, from to . As of , FDA records show no recalls naming K840566.

Clearance record

Decision date
Received
(289 days to decision)
Product code
JDR Staple, Fixation, Bone
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
3M Company Bldg.S 251-3 And 270, St. Paul MN
Third party review
No

Clearances, product code JDR

Trailing 12 months
2 clearances under product code JDR in the twelve months to October 2026, August 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JDR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20261
October 20260