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BIO-INTERFERENCE SCREW, 7 MM, 8 MM, 9 MM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971358
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1997
Days to Decision
89 days
Submission Type
Summary

BIO-INTERFERENCE SCREW, 7 MM, 8 MM, 9 MM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971358
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1997
Days to Decision
89 days
Submission Type
Summary