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FDA 510(k), K992239, PILLAR CHIN IMPLANT
FDA 510(k), K992239, PILLAR CHIN IMPLANT
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510(K) Number: K992239
Device Name: PILLAR CHIN IMPLANT
Manufacturer: PILLAR SURGICAL, INC.
Device Classification Name: prosthesis, chin, internal
Regulation Number: 878.3550
Classification Product Code: FWP
Date Received: 07/02/1999
Decision Date: 11/22/1999
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PILLAR CHIN IMPLANT
Manufacturer: PILLAR SURGICAL, INC.
Device Classification Name: prosthesis, chin, internal
Regulation Number: 878.3550
Classification Product Code: FWP
Date Received: 07/02/1999
Decision Date: 11/22/1999
Regulation Medical Specialty: General & Plastic Surgery
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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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