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ACROMED CANCELLOUS BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K860017
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
35 days

ACROMED CANCELLOUS BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K860017
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
35 days