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510(k) Data Aggregation
K Number
K962034Device Name
SC, CEMENTLESS HIP SYSTEM
Manufacturer
Date Cleared
1996-10-23
(152 days)
Product Code
Regulation Number
888.3360Why did this record match?
Applicant Name (Manufacturer) :
ARTOS MEDICAL PRODUCTS GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K962268Device Name
CHROME COBALT BALL HEAD
Manufacturer
Date Cleared
1996-10-23
(132 days)
Product Code
Regulation Number
888.3360Why did this record match?
Applicant Name (Manufacturer) :
ARTOS MEDICAL PRODUCTS GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K962086Device Name
CPS, CEMENTED CUP SYSTEM
Manufacturer
Date Cleared
1996-08-07
(70 days)
Product Code
Regulation Number
888.3350Why did this record match?
Applicant Name (Manufacturer) :
ARTOS MEDICAL PRODUCTS GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K961899Device Name
CPS, CEMENTED HIP SYSTEM
Manufacturer
Date Cleared
1996-08-01
(77 days)
Product Code
Regulation Number
888.3350Why did this record match?
Applicant Name (Manufacturer) :
ARTOS MEDICAL PRODUCTS GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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