KOENIG TOTAL TOE IMPLANT— 510(k) K884561

Name: FDA 510(k) clearance K884561
Creator: U.S. Food and Drug Administration
Published: 1989-01-24

Substantially Equivalent for Some Indications

Dow Corning Wright

FDA 510(k) clearance K884561 for KOENIG TOTAL TOE IMPLANT, Substantially Equivalent for Some Indications on 1989-01-24. Applicant: Dow Corning Wright. Device class: Unclassified.

Clearance details

Applicant: Dow Corning Wright
Product code: Code LZJ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1988-10-31
Decision date: 1989-01-24
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

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