FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Z - SERIES MODULAR TOTAL HIP SYSTEM PLASMA COATED

K Number: K040685 · Decision Jan 25, 2005
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
80
Applicant Total
21
Review Days
315

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Basic Information

Device Name
Z - SERIES MODULAR TOTAL HIP SYSTEM PLASMA COATED
K Number
K040685
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Osteoimplant Technology, Inc.
Date Received
March 16, 2004
Decision Date
January 25, 2005
Product Code
LWJ
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LWJ Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

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Other Clearances by Osteoimplant Technology, Inc.

K Number Device Name
K041443 OTI ALUMINA CERAMIC FEMORAL HEAD SYSTEM
K040225 OTI ALUMINA CERAMIC FEMORAL HEAD SYSTEM
K032729 Z-SERIES MODULAR TOTAL HIP SYSTEM
K030608 OTI BONE CEMENT PLUG
K022779 OTI UNICONDULAR INTERPOSITIONAL SPACER
K021822 R120 MODULAR TOTAL HIP SYSTEM
K012762 MJS POSTERIOR STABILIZED KNEE SYSTEM
K011774 R120 MODULAR TOTAL HIP SYSTEM
K003316 OTI CERAMIC FEMORAL HEAD SYSTEM
K003199 TRIAD II MODULAR TOTAL HIP SYSTEM
Search all 21 clearances from Osteoimplant Technology, Inc. →