510(k) K051306

HOFFMANN II MRI EXTERNAL FIXATION SYSTEM by Howmedica Osteonics Corp. — Product Code LXT

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