510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K103124Substantially Equivalent

Series II X3 Large Diameter Accetabular Inserts

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

K103124 is the FDA 510(k) clearance record for SERIES II X3 LARGE DIAMETER ACCETABULAR INSERTS, a class II device, cleared for Stryker Corporation on under FDA product code LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented). FDA records list 568 510(k) clearances for Stryker Corporation, from to . As of , FDA records show no recalls naming K103124.

Clearance record

Decision date
Received
(28 days to decision)
Product code
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Regulation
21 CFR 888.3358
Device class
Class II
Review panel
Orthopedic
Applicant
Stryker Corporation 325 Corporate Dr., Mahwah NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LPH

Trailing 12 months
9 clearances under product code LPH in the twelve months to November 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code LPH, trailing twelve months
MonthClearances
December 20251
January 20261
February 20261
March 20260
April 20260
May 20261
June 20261
July 20261
August 20262
September 20261
October 20260
November 20260