IMPLANT, H.P. CONDYLAR— 510(k) K781870

Substantially Equivalent

Dow Corning Corp. Healthcare Industries Materials

FDA 510(k) clearance K781870 for IMPLANT, H.P. CONDYLAR, Substantially Equivalent on 1979-02-09. Applicant: Dow Corning Corp. Healthcare Industries Materials.

Clearance details

Applicant: Dow Corning Corp. Healthcare Industries Materials
Product code: Code KWD
Advisory panel: Orthopedic
Date received: 1978-11-03
Decision date: 1979-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KWD

product code KWD

Injury: 164
Total: 164

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.