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OMNIFIT/OMNIFLEX/ODC/OMNIFIT-HA HIP STEM SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913812
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1991
Days to Decision
88 days
Submission Type
Summary

OMNIFIT/OMNIFLEX/ODC/OMNIFIT-HA HIP STEM SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913812
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1991
Days to Decision
88 days
Submission Type
Summary