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CRYSTALLINE BONE SCREW ENDO-OSSEOUS

Page Type
Cleared 510(K)
510(k) Number
K834364
510(k) Type
Traditional
Applicant
C.B.S. BIOTECHNICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1984
Days to Decision
131 days

CRYSTALLINE BONE SCREW ENDO-OSSEOUS

Page Type
Cleared 510(K)
510(k) Number
K834364
510(k) Type
Traditional
Applicant
C.B.S. BIOTECHNICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1984
Days to Decision
131 days