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HEMISPHERE MODULAR CUP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000321
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2000
Days to Decision
68 days
Submission Type
Statement

HEMISPHERE MODULAR CUP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000321
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2000
Days to Decision
68 days
Submission Type
Statement