STRYKER ORTHOPOWER 90 & ORTHOPOWER 90 SYSTEM II— 510(k) K863447

Name: FDA 510(k) clearance K863447
Creator: U.S. Food and Drug Administration
Published: 1986-09-29

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K863447 for STRYKER ORTHOPOWER 90 & ORTHOPOWER 90 SYSTEM II, Substantially Equivalent on 1986-09-29. Applicant: Stryker Corp.. Device class: 1.

Clearance details

Applicant: Stryker Corp.
Product code: Code GET
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1986-09-08
Decision date: 1986-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, 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.