FIXATION STAPLE KIT - DLIDE HAMMER— 510(k) K834515

Name: FDA 510(k) clearance K834515
Creator: U.S. Food and Drug Administration
Published: 1984-04-23

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K834515 for FIXATION STAPLE KIT - DLIDE HAMMER, Substantially Equivalent on 1984-04-23. Applicant: Stryker Corp.. Device class: 1.

Clearance details

Applicant: Stryker Corp.
Product code: Code HXJ
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1983-12-21
Decision date: 1984-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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