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CROSS CANCELLOUS BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896044
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/9/1989
Days to Decision
23 days

CROSS CANCELLOUS BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896044
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/9/1989
Days to Decision
23 days