OsteoProbe

Bone Indentation Device

Active Life Scientific, Inc.

The following data is part of a De Novo classification by Active Life Scientific, Inc. with the FDA for Osteoprobe.

Pre-market Notification Details

• DeNovo ID: DEN210013
• Device Name: OsteoProbe
• Classification: Bone Indentation Device
• Applicant: Active Life Scientific, Inc. 1027 Garden Street Santa Barbara, CA 93101
• Contact: Alexander Proctor
• Product Code: QGQ
• CFR Regulation Number: 888.1600 [🔎]
• Decision: Granted (DENG)
• 510(k) Premarket Notification: Device Classification Under Section 513(f)(2)(De Novo) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Lin
• Review Advisory Board: Orthopedic
• Classification Advisory: Orthopedic
• Type: Direct
• Date Received: 2021-03-30
• Decision Date: 2021-08-19
• Reclassification Order: Reclassification Order

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10860001719397	DEN210013	000