510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001471Substantially Equivalent

The Implex Hedrocel Acetabular Augment, Xx-Yyy-Zzzz

Implex Corp., Allendale NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001471 is the FDA 510(k) clearance record for THE IMPLEX HEDROCEL ACETABULAR AUGMENT, XX-YYY-ZZZZ, a class II device, cleared for Implex Corp. on under FDA product code LWJ (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented). FDA records list 65 510(k) clearances for Implex Corp., from to . As of , FDA records show no recalls naming K001471.

Clearance record

Decision date
Received
(88 days to decision)
Product code
LWJ Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
Regulation
21 CFR 888.3360
Device class
Class II
Review panel
Orthopedic
Applicant
Implex Corp. 80 Commerce Dr., Allendale NJ
510(k) summary
Summary
Third party review
No

Clearances, product code LWJ

Trailing 12 months

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

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