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Premia Spine XL Instruments

Page Type
Cleared 510(K)
510(k) Number
K191854
510(k) Type
Traditional
Applicant
Premia Spine, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/8/2019
Days to Decision
90 days
Submission Type
Summary

Premia Spine XL Instruments

Page Type
Cleared 510(K)
510(k) Number
K191854
510(k) Type
Traditional
Applicant
Premia Spine, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/8/2019
Days to Decision
90 days
Submission Type
Summary