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

OMEGA TOTAL HIP SYSTEM FOR CEMENTED APPLICATIONS

K Number: K960647 · Decision Sep 17, 1996
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
21
Review Days
215

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Basic Information

Device Name
OMEGA TOTAL HIP SYSTEM FOR CEMENTED APPLICATIONS
K Number
K960647
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Osteoimplant Technology, Inc.
Date Received
February 15, 1996
Decision Date
September 17, 1996
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Similar 510(k) Clearances

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Other Clearances by Osteoimplant Technology, Inc.

K Number Device Name
K040685 Z - SERIES MODULAR TOTAL HIP SYSTEM PLASMA COATED
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
Search all 21 clearances from Osteoimplant Technology, Inc. →