510(k) K012457
K012457 is an FDA 510(k) premarket notification submitted by Sodemsystems for the device "SODEM HIGH SPEED SYSTEM (ELECTRIC) (NEURO/SPINE SURGERY)". The FDA issued a decision of Substantially Equivalent on October 22, 2001. The device falls under product code HBC (Motor, Drill, Electric), a Class II device regulated under 21 CFR 882.4360. Sodemsystems has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 22, 2001
- Date Received
- August 1, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Motor, Drill, Electric
- Device Class
- Class II
- Regulation Number
- 882.4360
- Review Panel
- NE
- Submission Type