510(k) K931189

P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR ACET by Johnson & Johnson Orthopaedics, Inc. — Product Code LZO

K931189 is an FDA 510(k) premarket notification submitted by Johnson & Johnson Orthopaedics, Inc. for the device "P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR ACET". The FDA issued a decision of Substantially Equivalent on February 9, 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. Johnson & Johnson Orthopaedics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1994
Date Received
March 9, 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