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CORTICAL BONE SCREW (EUROPEAN STYLE)

Page Type
Cleared 510(K)
510(k) Number
K905357
510(k) Type
Traditional
Applicant
O'TEC CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/4/1991
Days to Decision
37 days

CORTICAL BONE SCREW (EUROPEAN STYLE)

Page Type
Cleared 510(K)
510(k) Number
K905357
510(k) Type
Traditional
Applicant
O'TEC CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/4/1991
Days to Decision
37 days