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ACROSSPINE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141695
510(k) Type
Traditional
Applicant
Arthro-Dif
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2014
Days to Decision
189 days
Submission Type
Summary

ACROSSPINE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141695
510(k) Type
Traditional
Applicant
Arthro-Dif
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2014
Days to Decision
189 days
Submission Type
Summary