MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004— 510(k) K050699

Name: FDA 510(k) clearance K050699
Creator: U.S. Food and Drug Administration
Published: 2005-04-15

Substantially Equivalent

Amedica Corp.

FDA 510(k) clearance K050699 for MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004, Substantially Equivalent on 2005-04-15. Applicant: Amedica Corp.. Device class: 2.

Clearance details

Applicant: Amedica Corp.
Product code: Product code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2005-03-18
Decision date: 2005-04-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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