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OMNIFLEX-C UHMWPE MID-SHAFT RESTRICTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923616
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1992
Days to Decision
101 days
Submission Type
Summary

OMNIFLEX-C UHMWPE MID-SHAFT RESTRICTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923616
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1992
Days to Decision
101 days
Submission Type
Summary