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FDA 510(k), K002063, BIOTRACE, MODEL 1730
FDA 510(k), K002063, BIOTRACE, MODEL 1730
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510(K) Number: K002063
Device Name: BIOTRACE, MODEL 1730
Manufacturer: BRYAN CORP.
Device Classification Name: accessory, barium sulfate, methyl methacrylate for cranioplasty
Regulation Number: 882.5300
Classification Product Code: MYU
Date Received: 07/07/2000
Decision Date: 08/10/2000
Regulation Medical Specialty: Neurology
Device Name: BIOTRACE, MODEL 1730
Manufacturer: BRYAN CORP.
Device Classification Name: accessory, barium sulfate, methyl methacrylate for cranioplasty
Regulation Number: 882.5300
Classification Product Code: MYU
Date Received: 07/07/2000
Decision Date: 08/10/2000
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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