STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR— 510(k) K981717

Name: FDA 510(k) clearance K981717
Creator: U.S. Food and Drug Administration
Published: 1998-06-30

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K981717 for STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR, Substantially Equivalent on 1998-06-30. Applicant: Stryker Instruments. Device class: 2.

Clearance details

Applicant: Stryker Instruments
Product code: Code FTD
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1998-05-15
Decision date: 1998-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FTD

product code FTD

Malfunction: 767
Total: 767

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.