510(k) K090240
K090240 is an FDA 510(k) premarket notification submitted by Monteris Medical, for the device "MONTERIS MEDICAL UFO". The FDA issued a decision of Substantially Equivalent on August 6, 2009. The device falls under product code HAW (Neurological Stereotaxic Instrument), a Class II device regulated under 21 CFR 882.4560. Monteris Medical, has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 6, 2009
- Date Received
- February 2, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Neurological Stereotaxic Instrument
- Device Class
- Class II
- Regulation Number
- 882.4560
- Review Panel
- NE
- Submission Type