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LIMITED ARTIFACT SKULL PIN, MODEL 0107

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073163
510(k) Type
Traditional
Applicant
Dinkler Surgical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2008
Days to Decision
111 days
Submission Type
Summary

LIMITED ARTIFACT SKULL PIN, MODEL 0107

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073163
510(k) Type
Traditional
Applicant
Dinkler Surgical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2008
Days to Decision
111 days
Submission Type
Summary