510(k) K223804
K223804 is an FDA 510(k) premarket notification submitted by Philips Ultrasound, LLC for the device "PercuNav Image Fusion and Interventional Navigation System". The FDA issued a decision of Substantially Equivalent on Jan 18, 2023. The device falls under product code JAK (System, X-Ray, Tomography, Computed), a Class II device regulated under 21 CFR 892.1750. Philips Ultrasound, LLC has 76 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 18, 2023
- Date Received
- Dec 19, 2022
- 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)