Last synced on 14 November 2025 at 11:06 pm

ACE CANCELLOUS BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K882831
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1988
Days to Decision
24 days

ACE CANCELLOUS BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K882831
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1988
Days to Decision
24 days