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
K173499Substantially Equivalent

Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads

Stryker Orthopaedics, Mahwah NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K173499 is the FDA 510(k) clearance record for Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads, a class II device, cleared for Stryker Orthopaedics on under FDA product code JDG (Prosthesis, Hip, Femoral Component, Cemented, Metal). FDA records list 24 510(k) clearances for Stryker Orthopaedics, from to . As of , FDA records show 2 recalls naming K173499.

Clearance record

Decision date
Received
(126 days to decision)
Product code
JDG Prosthesis, Hip, Femoral Component, Cemented, Metal
Regulation
21 CFR 888.3360
Device class
Class II
Review panel
Orthopedic
Applicant
Stryker Orthopaedics 325 Corporate Dr., Mahwah NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JDG

Trailing 12 months

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

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