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Pantheon Spinal Pontus Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K181548
510(k) Type
Traditional
Applicant
Pantheon Spinal
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2019
Days to Decision
552 days
Submission Type
Summary

Pantheon Spinal Pontus Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K181548
510(k) Type
Traditional
Applicant
Pantheon Spinal
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2019
Days to Decision
552 days
Submission Type
Summary