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FDA 510(k) K040417, PILLAR PALATAL IMPLANT SYSTEM, by Restore Medical, Inc.

FDA 510(k) K040417, PILLAR PALATAL IMPLANT SYSTEM, by Restore Medical, Inc.

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510(K) Number: K040417
Device Name: PILLAR PALATAL IMPLANT SYSTEM
Manufacturer: Restore Medical, Inc.
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 02/18/2004
Decision Date: 07/28/2004
Regulation Medical Specialty: Dental
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