HEMASORBPLUS press Resorable Hemostatic Bone Putty— 510(k) K143069

Name: FDA 510(k) clearance K143069
Creator: U.S. Food and Drug Administration
Published: 2014-12-22

Substantially Equivalent

Orthocon, Inc.

FDA 510(k) clearance K143069 for HEMASORBPLUS press Resorable Hemostatic Bone Putty, Substantially Equivalent on 2014-12-22. Applicant: Orthocon, Inc.. Device class: Unclassified.

Clearance details

Applicant: Orthocon, Inc.
Product code: Code MTJ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2014-10-27
Decision date: 2014-12-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Irvington, NY, US

Download summary PDF View on FDA.gov ↗

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