510(k) K041586

PROFEMUR S HIP STEM by Wrightmedicaltechnologyinc — Product Code JDL

K041586 is an FDA 510(k) premarket notification submitted by Wrightmedicaltechnologyinc for the device "PROFEMUR S HIP STEM". The FDA issued a decision of Substantially Equivalent on July 9, 2004. The device falls under product code JDL (Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)), a Class III device regulated under 21 CFR 888.3320. Wrightmedicaltechnologyinc has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 9, 2004
Date Received
June 14, 2004
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
Device Class
Class III
Regulation Number
888.3320
Review Panel
OR
Submission Type