510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062553Substantially Equivalent

Simplex P Bone Cement

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

K062553 is the FDA 510(k) clearance record for SIMPLEX P BONE CEMENT, a class II device, cleared for Stryker Orthopaedics on under FDA product code LOD (Bone Cement). FDA records list 24 510(k) clearances for Stryker Orthopaedics, from to . As of , FDA records show no recalls naming K062553.

Clearance record

Decision date
Received
(131 days to decision)
Product code
LOD Bone Cement
Regulation
21 CFR 888.3027
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 LOD

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