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PLUS PIVOT LINK UNIVERSAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K022271
510(k) Type
Traditional
Applicant
SPINEVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2002
Days to Decision
72 days
Submission Type
Summary

PLUS PIVOT LINK UNIVERSAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K022271
510(k) Type
Traditional
Applicant
SPINEVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2002
Days to Decision
72 days
Submission Type
Summary