ARTHROSTIM MANIPULATOR— 510(k) K930431

Name: FDA 510(k) clearance K930431
Creator: U.S. Food and Drug Administration
Published: 1994-07-15

Substantially Equivalent

Freeman Procedure Seminars

FDA 510(k) clearance K930431 for ARTHROSTIM MANIPULATOR, Substantially Equivalent on 1994-07-15. Applicant: Freeman Procedure Seminars. Device class: Unclassified.

Clearance details

Applicant: Freeman Procedure Seminars
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1993-01-26
Decision date: 1994-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salem, OR, US

Download summary PDF View on FDA.gov ↗

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