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FDA 510(k), K173188, The Graft Natural Bone Substitute
FDA 510(k), K173188, The Graft Natural Bone Substitute
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510(K) Number: K173188
Device Name: The Graft Natural Bone Substitute
Manufacturer: Purgo Biologics Inc.
Device Classification Name: bone grafting material, animal source
Regulation Number: 872.3930
Classification Product Code: NPM
Date Received: 10/02/2017
Decision Date: 07/20/2018
Regulation Medical Specialty: Dental
Device Name: The Graft Natural Bone Substitute
Manufacturer: Purgo Biologics Inc.
Device Classification Name: bone grafting material, animal source
Regulation Number: 872.3930
Classification Product Code: NPM
Date Received: 10/02/2017
Decision Date: 07/20/2018
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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