510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842234Substantially Equivalent

New Jersey Femoral Stem

Endomedics, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842234 is the FDA 510(k) clearance record for NEW JERSEY FEMORAL STEM, a class II device, cleared for Endomedics, Inc. on under FDA product code KWL (Prosthesis, Hip, Hemi-, Femoral, Metal). FDA records list 4 510(k) clearances for Endomedics, Inc., from to . As of , FDA records show 3 recalls naming K842234.

Clearance record

Decision date
Received
(45 days to decision)
Product code
KWL Prosthesis, Hip, Hemi-, Femoral, Metal
Regulation
21 CFR 888.3360
Device class
Class II
Review panel
Orthopedic
Applicant
Endomedics, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code KWL

Trailing 12 months
3 clearances under product code KWL in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KWL, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20261
August 20260
September 20260
October 20260