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ORTHO-PRO CANNULATED BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K042310
510(k) Type
Traditional
Applicant
ORTHO-PRO LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2004
Days to Decision
22 days
Submission Type
Summary

ORTHO-PRO CANNULATED BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K042310
510(k) Type
Traditional
Applicant
ORTHO-PRO LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2004
Days to Decision
22 days
Submission Type
Summary