510(k) K051856
K051856 is an FDA 510(k) premarket notification submitted by Trans1 Incorporated for the device "TRANS1 FACET SCREWS". The FDA issued a decision of Substantially Equivalent on Sep 26, 2005. The device falls under product code MRW (System, Facet Screw Spinal Device), a Class U device. Trans1 Incorporated has 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 26, 2005
- Date Received
- Jul 8, 2005
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Facet Screw Spinal Device
- Device Class
- Class U
- Review Panel
- OR
- Submission Type
- 510(k)