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FDA 510(k), K990498, OPTIBOND SOLO PLUS
FDA 510(k), K990498, OPTIBOND SOLO PLUS
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510(K) Number: K990498
Device Name: OPTIBOND SOLO PLUS
Manufacturer: SYBRON DENTAL SPECIALTIES, INC.
Device Classification Name: agent, tooth bonding, resin
Regulation Number: 872.3200
Classification Product Code: KLE
Date Received: 02/17/1999
Decision Date: 03/08/1999
Regulation Medical Specialty: Dental
Device Name: OPTIBOND SOLO PLUS
Manufacturer: SYBRON DENTAL SPECIALTIES, INC.
Device Classification Name: agent, tooth bonding, resin
Regulation Number: 872.3200
Classification Product Code: KLE
Date Received: 02/17/1999
Decision Date: 03/08/1999
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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