510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K881779Substantially Equivalent for Some Indications

Whiteside Ortholoc II Unicondylar Knee System

Dow Corning Wright, Arlington TN / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K881779 is the FDA 510(k) clearance record for WHITESIDE ORTHOLOC II UNICONDYLAR KNEE SYSTEM, a class II device, cleared for Dow Corning Wright on under FDA product code HSX (Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer). FDA records list 74 510(k) clearances for Dow Corning Wright, from to . As of , FDA records show no recalls naming K881779.

Clearance record

Decision date
Received
(127 days to decision)
Product code
HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Regulation
21 CFR 888.3520
Device class
Class II
Review panel
Orthopedic
Applicant
Dow Corning Wright P.O. Box 100, Arlington TN
Third party review
No

Clearances, product code HSX

Trailing 12 months
2 clearances under product code HSX 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 HSX, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260