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PREMIER 7000 CTL SPINE COIL

Page Type
Cleared 510(K)
510(k) Number
K980157
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1998
Days to Decision
87 days
Submission Type
Summary

PREMIER 7000 CTL SPINE COIL

Page Type
Cleared 510(K)
510(k) Number
K980157
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1998
Days to Decision
87 days
Submission Type
Summary