Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K083912Substantially Equivalent

Treu; Bone Screws, Schanz Screws, Kirschner Wires, Steinmann Pins, Larsen Pins

Treu-Instrumente GmbH, Mühlheim An Der Donau, DE / Traditional, Substantially Equivalent

K083912 is the FDA 510(k) clearance record for TREU; BONE SCREWS, SCHANZ SCREWS, KIRSCHNER WIRES, STEINMANN PINS, LARSEN PINS, a class II device, cleared for Treu-Instrumente GmbH on under FDA product code HWC (Screw, Fixation, Bone). FDA records list one 510(k) clearance for Treu-Instrumente GmbH. As of , FDA records show no recalls naming K083912.

Clearance record

Decision date
Received
(197 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Treu-Instrumente GmbH Griesweg 47, Mühlheim An Der Donau, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HWC

Trailing 12 months
22 clearances under product code HWC in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code HWC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20262
April 20263
May 20264
June 20262
July 20261
August 20263
September 20264
October 20261