Last synced on 14 November 2025 at 11:06 pm

SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial Implant

Page Type
Cleared 510(K)
510(k) Number
K152463
510(k) Type
Traditional
Applicant
PORIFEROUS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
145 days
Submission Type
Summary

SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial Implant

Page Type
Cleared 510(K)
510(k) Number
K152463
510(k) Type
Traditional
Applicant
PORIFEROUS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
145 days
Submission Type
Summary