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FDA 510(k), K101423, OPTIBOND XTR
FDA 510(k), K101423, OPTIBOND XTR
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$149.00 USD
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$149.00 USD
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510(K) Number: K101423
Device Name: OPTIBOND XTR
Manufacturer: KERR CORPORATION
Device Classification Name: agent, tooth bonding, resin
Regulation Number: 872.3200
Classification Product Code: KLE
Date Received: 05/20/2010
Decision Date: 07/30/2010
Regulation Medical Specialty: Dental
Device Name: OPTIBOND XTR
Manufacturer: KERR CORPORATION
Device Classification Name: agent, tooth bonding, resin
Regulation Number: 872.3200
Classification Product Code: KLE
Date Received: 05/20/2010
Decision Date: 07/30/2010
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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