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FDA 510(k), K905129, BAERVELDT GLAUCOMA IMPLANT
FDA 510(k), K905129, BAERVELDT GLAUCOMA IMPLANT
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510(K) Number: K905129
Device Name: BAERVELDT GLAUCOMA IMPLANT
Manufacturer: WRIGHT MEDICAL CORP.
Device Classification Name: implant, eye valve
Regulation Number: 886.3920
Classification Product Code: KYF
Date Received: 11/14/1990
Decision Date: 02/11/1991
Regulation Medical Specialty: Ophthalmic
Device Name: BAERVELDT GLAUCOMA IMPLANT
Manufacturer: WRIGHT MEDICAL CORP.
Device Classification Name: implant, eye valve
Regulation Number: 886.3920
Classification Product Code: KYF
Date Received: 11/14/1990
Decision Date: 02/11/1991
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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