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FDA 510(k), K923419, TISMESH SYSTEM
FDA 510(k), K923419, TISMESH SYSTEM
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510(K) Number: K923419
Device Name: TISMESH SYSTEM
Manufacturer: TI-MESH, INC.
Device Classification Name: plate, bone
Regulation Number: 872.4760
Classification Product Code: JEY
Date Received: 07/13/1992
Decision Date: 04/08/1993
Regulation Medical Specialty: Dental
Device Name: TISMESH SYSTEM
Manufacturer: TI-MESH, INC.
Device Classification Name: plate, bone
Regulation Number: 872.4760
Classification Product Code: JEY
Date Received: 07/13/1992
Decision Date: 04/08/1993
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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