Last synced on 30 September 2022 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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