510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K904870Substantially Equivalent

Modified New Jersey Femoral Hip Resurfacing Compon

Endotec, Inc., South Orange NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K904870 is the FDA 510(k) clearance record for MODIFIED NEW JERSEY FEMORAL HIP RESURFACING COMPON, a class II device, cleared for Endotec, Inc. on under FDA product code KXA (Prosthesis, Hip, Femoral, Resurfacing). FDA records list 15 510(k) clearances for Endotec, Inc., from to . As of , FDA records show 3 recalls naming K904870.

Clearance record

Decision date
Received
(212 days to decision)
Product code
KXA Prosthesis, Hip, Femoral, Resurfacing
Regulation
21 CFR 888.3400
Device class
Class II
Review panel
Orthopedic
Applicant
Endotec, Inc. 20 Valley St., South Orange NJ
Third party review
No

Clearances, product code KXA

Trailing 12 months

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

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