510(k) K051306
K051306 is an FDA 510(k) premarket notification submitted by Howmedica Osteonics Corp. for the device "HOFFMANN II MRI EXTERNAL FIXATION SYSTEM". The FDA issued a decision of Substantially Equivalent on June 17, 2005. The device falls under product code LXT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite), a Class II device regulated under 21 CFR 888.3030. Howmedica Osteonics Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 17, 2005
- Date Received
- May 19, 2005
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type