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OMNISPAN MENISCAL REPAIR SYSTEM/0 DEGREE, MODEL 228140, RAPIDLOC A2 MENISCAL REPAIR SYSTEM/12 DEGREE, MODEL 228141

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092836
510(k) Type
Traditional
Applicant
Depuy Mitek, A Johnson & Johnson Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2010
Days to Decision
142 days
Submission Type
Summary

OMNISPAN MENISCAL REPAIR SYSTEM/0 DEGREE, MODEL 228140, RAPIDLOC A2 MENISCAL REPAIR SYSTEM/12 DEGREE, MODEL 228141

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092836
510(k) Type
Traditional
Applicant
Depuy Mitek, A Johnson & Johnson Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2010
Days to Decision
142 days
Submission Type
Summary