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AMSET(TM) CANNULATED BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931538
510(k) Type
Traditional
Applicant
ADVANCED MED/SURG, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/4/1994
Days to Decision
401 days
Submission Type
Statement

AMSET(TM) CANNULATED BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931538
510(k) Type
Traditional
Applicant
ADVANCED MED/SURG, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/4/1994
Days to Decision
401 days
Submission Type
Statement