510(k) K220595
K220595 is an FDA 510(k) premarket notification submitted by Neodynamics AB for the device "NeoNavia Biopsy System". The FDA issued a decision of Substantially Equivalent on Sep 8, 2022. The device falls under product code KNW (Instrument, Biopsy), a Class II device regulated under 21 CFR 876.1075.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 8, 2022
- Date Received
- Mar 1, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instrument, Biopsy
- Device Class
- Class II
- Regulation Number
- 876.1075
- Review Panel
- SU
- Submission Type
- 510(k)