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FDA 510(k), K082924, DYNASTY POROUS ACETABULAR SHELL, DYNASTY POLYETHYLENE ACETABULAR LINER, DYNASTY METAL ACETABULAR LINER
FDA 510(k), K082924, DYNASTY POROUS ACETABULAR SHELL, DYNASTY POLYETHYLENE ACETABULAR LINER, DYNASTY METAL ACETABULAR LINER
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510(K) Number: K082924
Device Name: DYNASTY POROUS ACETABULAR SHELL, DYNASTY POLYETHYLENE ACETABULAR LINER, DYNASTY METAL ACETABULAR LINER
Manufacturer: WRIGHT MEDICAL TECHNOLOGY, INC.
Device Classification Name: prosthesis, hip, semi-constrained (metal uncemented acetabular component)
Regulation Number: 888.3330
Classification Product Code: KWA
Date Received: 10/01/2008
Decision Date: 03/06/2009
Regulation Medical Specialty: Orthopedic
Device Name: DYNASTY POROUS ACETABULAR SHELL, DYNASTY POLYETHYLENE ACETABULAR LINER, DYNASTY METAL ACETABULAR LINER
Manufacturer: WRIGHT MEDICAL TECHNOLOGY, INC.
Device Classification Name: prosthesis, hip, semi-constrained (metal uncemented acetabular component)
Regulation Number: 888.3330
Classification Product Code: KWA
Date Received: 10/01/2008
Decision Date: 03/06/2009
Regulation Medical Specialty: Orthopedic
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