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MODULAR ACETABULAR SHELL II

Page Type
Cleared 510(K)
510(k) Number
K955739
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1996
Days to Decision
100 days
Submission Type
Summary

MODULAR ACETABULAR SHELL II

Page Type
Cleared 510(K)
510(k) Number
K955739
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1996
Days to Decision
100 days
Submission Type
Summary