Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K252824Substantially Equivalent

Evolve AP Cup, World Finned Cup, World G-Zero Liner and Oddball Femoral Head

Signature Orthopaedics Pty Limited, Lane Cove West, AU / Traditional, Substantially Equivalent

K252824 is the FDA 510(k) clearance record for Evolve AP Cup, World Finned Cup, World G-Zero Liner and Oddball Femoral Head, a class II device, cleared for Signature Orthopaedics Pty, Ltd. on under FDA product code JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented). FDA records list 45 510(k) clearances for Signature Orthopaedics Pty, Ltd., from to . As of , FDA records show no recalls naming K252824.

Clearance record

Decision date
Received
(188 days to decision)
Product code
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Regulation
21 CFR 888.3350
Device class
Class II
Review panel
Orthopedic
Applicant
Signature Orthopaedics Pty, Ltd. 7 Sirius Rd., Lane Cove West, AU
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JDI

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