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MODIFICATION TO HBS HEADLESS BONE SCREW

Page Type
Cleared 510(K)
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)
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