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

Name: FDA 510(k) clearance K781870
Creator: U.S. Food and Drug Administration
Published: 1979-02-09

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. Device class: 2.

Clearance details

Applicant: Dow Corning Corp. Healthcare Industries Materials
Product code: Code KWD
Device class: Class 2
Regulation: 21 CFR 888.3730
Advisory panel: Orthopedic
Date received: 1978-11-03
Decision date: 1979-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K850255 — DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET1985-05-01
K843995 — TF-II HIP PROSTHESIS1985-04-23
K842559 — WHITESIDE ORTHOLOC TOTAL HIP FEMORAL1984-12-20

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.