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

SIMPLEX X

K Number: K032945 · Decision May 25, 2004
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
71
Applicant Total
124
Review Days
246

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Basic Information

Device Name
SIMPLEX X
K Number
K032945
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corp.
Date Received
September 22, 2003
Decision Date
May 25, 2004
Product Code
LOD
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
LOD Bone Cement

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