510(k) K002693
K002693 is an FDA 510(k) premarket notification submitted by Cbs Intl. B.V. for the device "CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)". The FDA issued a decision of Substantially Equivalent on November 9, 2000. The device falls under product code EBL (Pin, Retentive And Splinting, And Accessory Instruments), a Class I device regulated under 21 CFR 872.3740.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 9, 2000
- Date Received
- August 29, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pin, Retentive And Splinting, And Accessory Instruments
- Device Class
- Class I
- Regulation Number
- 872.3740
- Review Panel
- DE
- Submission Type