510(k) K121476
K121476 is an FDA 510(k) premarket notification submitted by Pinnacle Spine Group, LLC for the device "INFILL GRAFT DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on Aug 29, 2012. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Pinnacle Spine Group, LLC has 12 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 29, 2012
- Date Received
- May 18, 2012
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Piston
- Device Class
- Class II
- Regulation Number
- 880.5860
- Review Panel
- HO
- Submission Type
- 510(k)