510(k) K003500
K003500 is an FDA 510(k) premarket notification submitted by Rebstock - Instrumente GmbH for the device "REBSTOCK YASARGIL ANEURYSM CLIP". The FDA issued a decision of Substantially Equivalent on May 30, 2001. The device falls under product code HCH (Clip, Aneurysm), a Class II device regulated under 21 CFR 882.5200.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 30, 2001
- Date Received
- November 13, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clip, Aneurysm
- Device Class
- Class II
- Regulation Number
- 882.5200
- Review Panel
- NE
- Submission Type