510(k) K170716
K170716 is an FDA 510(k) premarket notification submitted by Philips Ultrasound, Inc. for the device "PercuNav Image Fusion and Interventional Navigation". The FDA issued a decision of Substantially Equivalent on Apr 21, 2017. The device falls under product code JAK (System, X-Ray, Tomography, Computed), a Class II device regulated under 21 CFR 892.1750. Philips Ultrasound, Inc. has 76 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 21, 2017
- Date Received
- Mar 9, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, X-Ray, Tomography, Computed
- Device Class
- Class II
- Regulation Number
- 892.1750
- Review Panel
- RA
- Submission Type
- 510(k)