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ULTIMAX CORTICAL BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K990513
510(k) Type
Traditional
Applicant
BIODYNAMIC TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1999
Days to Decision
27 days
Submission Type
Statement

ULTIMAX CORTICAL BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K990513
510(k) Type
Traditional
Applicant
BIODYNAMIC TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1999
Days to Decision
27 days
Submission Type
Statement