510(k) K933567

EUROFORM TOTAL HIP PROSTHESIS by Landos, Inc. — Product Code LZO

K933567 is an FDA 510(k) premarket notification submitted by Landos, Inc. for the device "EUROFORM TOTAL HIP PROSTHESIS". The FDA issued a decision of SN on May 16, 1994. The device falls under product code LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented), a Class II device regulated under 21 CFR 888.3353. Landos, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
May 16, 1994
Date Received
July 22, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device Class
Class II
Regulation Number
888.3353
Review Panel
OR
Submission Type