510(k) K062821
K062821 is an FDA 510(k) premarket notification submitted by Medtronic Neurosurgery for the device "U-CLIP DEVICE". The FDA issued a decision of Substantially Equivalent on December 19, 2006. The device falls under product code FZP (Clip, Implantable), a Class II device regulated under 21 CFR 878.4300. Medtronic Neurosurgery has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 19, 2006
- Date Received
- September 20, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clip, Implantable
- Device Class
- Class II
- Regulation Number
- 878.4300
- Review Panel
- SU
- Submission Type