510(k) K024040
K024040 is an FDA 510(k) premarket notification submitted by Phoenix Biomedical Corp. for the device "ACCURA ELITE SHUNT SYSTEM". The FDA issued a decision of Substantially Equivalent on January 27, 2003. The device falls under product code JXG (Shunt, Central Nervous System And Components), a Class II device regulated under 21 CFR 882.5550. Phoenix Biomedical Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 27, 2003
- Date Received
- December 6, 2002
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Shunt, Central Nervous System And Components
- Device Class
- Class II
- Regulation Number
- 882.5550
- Review Panel
- NE
- Submission Type