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OMNIAXIAL CONNECTOR

Page Type
Cleared 510(K)
510(k) Number
K993926
510(k) Type
Special
Applicant
ORTHOTEC, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1999
Days to Decision
29 days
Submission Type
Summary

OMNIAXIAL CONNECTOR

Page Type
Cleared 510(K)
510(k) Number
K993926
510(k) Type
Special
Applicant
ORTHOTEC, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1999
Days to Decision
29 days
Submission Type
Summary