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TITANIUM ALLOY BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K970549
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
4/30/1997
Days to Decision
77 days

TITANIUM ALLOY BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K970549
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
4/30/1997
Days to Decision
77 days