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EXTREMITY BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963118
510(k) Type
Traditional
Applicant
ACUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/10/1996
Days to Decision
59 days

EXTREMITY BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963118
510(k) Type
Traditional
Applicant
ACUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/10/1996
Days to Decision
59 days