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

LEGEND ALL-POLY CUP

K Number: K051407 · Decision Sep 8, 2005
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
45
Review Days
100

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Basic Information

Device Name
LEGEND ALL-POLY CUP
K Number
K051407
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ortho Development Corp.
Date Received
May 31, 2005
Decision Date
September 8, 2005
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

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