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NEXLINK OCT SYSTEM, MODEL 7000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K090060
510(k) Type
Traditional
Applicant
ABBOTT SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2009
Days to Decision
144 days
Submission Type
Summary

NEXLINK OCT SYSTEM, MODEL 7000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K090060
510(k) Type
Traditional
Applicant
ABBOTT SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2009
Days to Decision
144 days
Submission Type
Summary