510(k) K161234
K161234 is an FDA 510(k) premarket notification submitted by Scion Medical Technologies, LLC for the device "CASSI II Rotational Core Biopsy System". The FDA issued a decision of Substantially Equivalent on Aug 3, 2016. The device falls under product code KNW (Instrument, Biopsy), a Class II device regulated under 21 CFR 876.1075. Scion Medical Technologies, LLC has 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 3, 2016
- Date Received
- May 2, 2016
- Clearance Type
- Special
- 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)