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VEGA KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101281
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2010
Days to Decision
85 days
Submission Type
Summary

VEGA KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101281
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2010
Days to Decision
85 days
Submission Type
Summary