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
K142052Substantially Equivalent

Orthofix Galaxy Unyco Diaphyseal Tibia Kit

Orthofix SRL, Wilmington NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K142052 is the FDA 510(k) clearance record for ORTHOFIX GALAXY UNYCO DIAPHYSEAL TIBIA KIT, a class II device, cleared for Orthofix Srl on under FDA product code KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component). FDA records list 102 510(k) clearances for Orthofix Srl, from to . As of , FDA records show one recall naming K142052.

Clearance record

Decision date
Received
(130 days to decision)
Product code
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Orthofix Srl P.O. Box 15729, Wilmington NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KTT

Trailing 12 months
9 clearances under product code KTT in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KTT, trailing twelve months
MonthClearances
November 20252
December 20252
January 20261
February 20260
March 20261
April 20261
May 20260
June 20261
July 20260
August 20260
September 20260
October 20261