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MODIFICATION TO HBS HEADLESS BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101030
510(k) Type
Special
Applicant
Biopro, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2010
Days to Decision
51 days
Submission Type
Summary

MODIFICATION TO HBS HEADLESS BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101030
510(k) Type
Special
Applicant
Biopro, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2010
Days to Decision
51 days
Submission Type
Summary