510(k) K901480

F-20 TOTAL HIP PROSTHESIS by Med-Tek Corp. — Product Code JDI

K901480 is an FDA 510(k) premarket notification submitted by Med-Tek Corp. for the device "F-20 TOTAL HIP PROSTHESIS". The FDA issued a decision of Substantially Equivalent on June 12, 1990. The device falls under product code JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented), a Class II device regulated under 21 CFR 888.3350. Med-Tek Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 12, 1990
Date Received
March 27, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device Class
Class II
Regulation Number
888.3350
Review Panel
OR
Submission Type