Last synced on 4 February 2023 at 10:33 pm

POREX(TM) EYE SPHERE IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863943
510(k) Type
Traditional
Applicant
POREX MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1987
Days to Decision
140 days

POREX(TM) EYE SPHERE IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863943
510(k) Type
Traditional
Applicant
POREX MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1987
Days to Decision
140 days