ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE— 510(k) K092044

Name: FDA 510(k) clearance K092044
Creator: U.S. Food and Drug Administration
Published: 2009-12-18

Substantially Equivalent

Orthocor Medical

FDA 510(k) clearance K092044 for ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE, Substantially Equivalent on 2009-12-18. Applicant: Orthocor Medical. Device class: 2.

Clearance details

Applicant: Orthocor Medical
Product code: Code ILX
Device class: Class 2
Regulation: 21 CFR 890.5290
Advisory panel: Physical Medicine
Date received: 2009-07-06
Decision date: 2009-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mccordsville, IN, US

Download summary PDF View on FDA.gov ↗

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