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CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K943474
510(k) Type
Traditional
Applicant
COHORT MEDICAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1994
Days to Decision
87 days
Submission Type
Statement

CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K943474
510(k) Type
Traditional
Applicant
COHORT MEDICAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1994
Days to Decision
87 days
Submission Type
Statement