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FDA 510(k), K091120, MEDPOR CONTAIN IMPLANT
FDA 510(k), K091120, MEDPOR CONTAIN IMPLANT
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510(K) Number: K091120
Device Name: MEDPOR CONTAIN IMPLANT
Manufacturer: JERRI L MANN
Device Classification Name: Barrier, Synthetic, Intraoral
Regulation Number: NPK
Classification Product Code: 04/17/2009
Date Received: 03/19/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: MEDPOR CONTAIN IMPLANT
Manufacturer: JERRI L MANN
Device Classification Name: Barrier, Synthetic, Intraoral
Regulation Number: NPK
Classification Product Code: 04/17/2009
Date Received: 03/19/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
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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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