InterOss— 510(k) K151209

Substantially Equivalent

Sigmagraft, Inc.

FDA 510(k) clearance K151209 for InterOss, Substantially Equivalent on 2015-11-06. Applicant: Sigmagraft, Inc..

Clearance details

Applicant: Sigmagraft, Inc.
Product code: Code NPM
Advisory panel: Dental
Date received: 2015-05-06
Decision date: 2015-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

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