510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842559Substantially Equivalent

Whiteside Ortholoc Total Hip Femoral

Dow Corning Corp. Healthcare Industries Materials, P.O. Box 1767 Midland MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842559 is the FDA 510(k) clearance record for WHITESIDE ORTHOLOC TOTAL HIP FEMORAL, a class II device, cleared for Dow Corning Corp. Healthcare Industries Materials on under FDA product code KWL (Prosthesis, Hip, Hemi-, Femoral, Metal). FDA records list 31 510(k) clearances for Dow Corning Corp. Healthcare Industries Materials, from to . As of , FDA records show no recalls naming K842559.

Clearance record

Decision date
Received
(171 days to decision)
Product code
KWL Prosthesis, Hip, Hemi-, Femoral, Metal
Regulation
21 CFR 888.3360
Device class
Class II
Review panel
Orthopedic
Applicant
Dow Corning Corp. Healthcare Industries Materials
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