WHITESIDE ORTHOLOC II UNICONDYLAR KNEE SYSTEM— 510(k) K881779

Substantially Equivalent for Some Indications

Dow Corning Wright

FDA 510(k) clearance K881779 for WHITESIDE ORTHOLOC II UNICONDYLAR KNEE SYSTEM, Substantially Equivalent for Some Indications on 1988-08-31. Applicant: Dow Corning Wright.

Clearance details

Applicant: Dow Corning Wright
Product code: Code HSX
Advisory panel: Orthopedic
Date received: 1988-04-26
Decision date: 1988-08-31
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HSX

product code HSX

Injury: 1,003
Other: 1
Total: 1,004

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.