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PLASMAFIT ACETABULAR CUP AND VITELENE INSERT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122783
510(k) Type
Traditional
Applicant
Aesculap Implant System, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2013
Days to Decision
414 days
Submission Type
Summary

PLASMAFIT ACETABULAR CUP AND VITELENE INSERT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122783
510(k) Type
Traditional
Applicant
Aesculap Implant System, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2013
Days to Decision
414 days
Submission Type
Summary