510(k) K062978

U2 HIP STEM, TI PLASMA SPRAY by United Orthopedic Corp. — Product Code LWJ

K062978 is an FDA 510(k) premarket notification submitted by United Orthopedic Corp. for the device "U2 HIP STEM, TI PLASMA SPRAY". The FDA issued a decision of Substantially Equivalent on January 16, 2007. The device falls under product code LWJ (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented), a Class II device regulated under 21 CFR 888.3360. United Orthopedic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 16, 2007
Date Received
September 29, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
Device Class
Class II
Regulation Number
888.3360
Review Panel
OR
Submission Type