510(k) K040630

TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ by Implex Corp. — Product Code JWH

K040630 is an FDA 510(k) premarket notification submitted by Implex Corp. for the device "TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ". The FDA issued a decision of Substantially Equivalent on September 30, 2004. The device falls under product code JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer), a Class II device regulated under 21 CFR 888.3560. Implex Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 2004
Date Received
March 10, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device Class
Class II
Regulation Number
888.3560
Review Panel
OR
Submission Type