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FDA 510(k), K071732, MARROWMINER
FDA 510(k), K071732, MARROWMINER
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510(K) Number: K071732
Device Name: MARROWMINER
Manufacturer: STEMCOR SYSTEMS, INC.
Device Classification Name: needle, aspiration and injection, reusable
Regulation Number: 878.4800
Classification Product Code: GDM
Date Received: 06/26/2007
Decision Date: 09/24/2007
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MARROWMINER
Manufacturer: STEMCOR SYSTEMS, INC.
Device Classification Name: needle, aspiration and injection, reusable
Regulation Number: 878.4800
Classification Product Code: GDM
Date Received: 06/26/2007
Decision Date: 09/24/2007
Regulation Medical Specialty: General & Plastic Surgery
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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. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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