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FDA 510(k), K063527, MBCP+
FDA 510(k), K063527, MBCP+
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510(K) Number: K063527
Device Name: MBCP+
Manufacturer: BIOMATLANTE
Device Classification Name: filler, bone void, calcium compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 11/22/2006
Decision Date: 07/30/2007
Regulation Medical Specialty: Orthopedic
Device Name: MBCP+
Manufacturer: BIOMATLANTE
Device Classification Name: filler, bone void, calcium compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 11/22/2006
Decision Date: 07/30/2007
Regulation Medical Specialty: Orthopedic
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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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