510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K930431Substantially Equivalent

Arthrostim Manipulator

Freeman Procedure Seminars, Salem OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930431 is the FDA 510(k) clearance record for ARTHROSTIM MANIPULATOR, cleared for Freeman Procedure Seminars on under FDA product code LXM (Manipulator, Plunger-Like Joint). FDA records list one 510(k) clearance for Freeman Procedure Seminars. As of , FDA records show no recalls naming K930431.

Clearance record

Decision date
Received
(535 days to decision)
Product code
LXM Manipulator, Plunger-Like Joint
Device class
Unclassified
Review panel
Unknown
Applicant
Freeman Procedure Seminars 4747 River Rd. N., Salem OR
510(k) summary
Summary
Third party review
No

Clearances, product code LXM

Trailing 12 months

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

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