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LINK, ACETABULAR REVISION MESH CUP

Page Type
Cleared 510(K)
510(k) Number
K972760
510(k) Type
Traditional
Applicant
Link America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1997
Days to Decision
90 days
Submission Type
Statement

LINK, ACETABULAR REVISION MESH CUP

Page Type
Cleared 510(K)
510(k) Number
K972760
510(k) Type
Traditional
Applicant
Link America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1997
Days to Decision
90 days
Submission Type
Statement