510(k) K230836
K230836 is an FDA 510(k) premarket notification submitted by Surgmark GmbH for the device "SchurSign Tissue Marker". The FDA issued a decision of Substantially Equivalent on January 23, 2024. The device falls under product code NEU (Marker, Radiographic, Implantable), a Class II device regulated under 21 CFR 878.4300.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 23, 2024
- Date Received
- March 27, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Marker, Radiographic, Implantable
- Device Class
- Class II
- Regulation Number
- 878.4300
- Review Panel
- SU
- Submission Type