FDA 510(k), K040417, PILLAR PALATAL IMPLANT SYSTEM
FDA 510(k), K040417, PILLAR PALATAL IMPLANT SYSTEM
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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
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