510(k) K032905

3DKNEE POROUS COATED FEMORAL COMPONENT by Encore Orthopedics, Inc. — Product Code MBH

K032905 is an FDA 510(k) premarket notification submitted by Encore Orthopedics, Inc. for the device "3DKNEE POROUS COATED FEMORAL COMPONENT". The FDA issued a decision of Substantially Equivalent on July 6, 2004. The device falls under product code MBH (Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer), a Class II device regulated under 21 CFR 888.3565. Encore Orthopedics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 6, 2004
Date Received
September 17, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Device Class
Class II
Regulation Number
888.3565
Review Panel
OR
Submission Type