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EXTREMITY BONE SCREW

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