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
K002324Substantially Equivalent

Modified to Modular Fr Severe Bone Loss Trauma

Sulzermedica, Austin TX / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K002324 is the FDA 510(k) clearance record for MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA, a class II device, cleared for Sulzermedica on under FDA product code JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented). FDA records list 5 510(k) clearances for Sulzermedica, from to . As of , FDA records show one recall naming K002324.

Clearance record

Decision date
Received
(24 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
Sulzermedica 9900 Spectrum Dr., Austin TX
510(k) summary
Summary
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