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STRYKER VERTAPLEX RADIOPAQUE BONE CEMENT

Page Type
Cleared 510(K)
510(k) Number
K072118
510(k) Type
Traditional
Applicant
STRYKER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2007
Days to Decision
128 days
Submission Type
Summary

STRYKER VERTAPLEX RADIOPAQUE BONE CEMENT

Page Type
Cleared 510(K)
510(k) Number
K072118
510(k) Type
Traditional
Applicant
STRYKER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2007
Days to Decision
128 days
Submission Type
Summary