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RIGIDFIX BIOCRYL 2.7MM BTB (210815), FEMORAL 3.3MM ST (210816), AND TIBIAL 3.3MM ST (210817) CROSS PIN KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091041
510(k) Type
Traditional
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2009
Days to Decision
116 days
Submission Type
Summary

RIGIDFIX BIOCRYL 2.7MM BTB (210815), FEMORAL 3.3MM ST (210816), AND TIBIAL 3.3MM ST (210817) CROSS PIN KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091041
510(k) Type
Traditional
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2009
Days to Decision
116 days
Submission Type
Summary