510(k) K161406
K161406 is an FDA 510(k) premarket notification submitted by Claronav, Inc. for the device "Navident". The FDA issued a decision of Substantially Equivalent on September 8, 2016. The device falls under product code PLV (Dental Stereotaxic Instrument), a Class II device regulated under 21 CFR 872.4120. Claronav, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 8, 2016
- Date Received
- May 20, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dental Stereotaxic Instrument
- Device Class
- Class II
- Regulation Number
- 872.4120
- Review Panel
- DE
- Submission Type
To facilitate dental implant placement in patients that are partially endentulous or edentulous.