POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT

Implant, Orbital, Extra-ocular

POREX MEDICAL

The following data is part of a premarket notification filed by Porex Medical with the FDA for Porex(tm) Extra-ocular Orbital Implant.

Pre-market Notification Details

Device IDK863946
510k NumberK863946
Device Name:POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT
ClassificationImplant, Orbital, Extra-ocular
Applicant POREX MEDICAL 500 BOHANNON RD. Fairburn,  GA  30213
ContactHoward A Mercer,phd
CorrespondentHoward A Mercer,phd
POREX MEDICAL 500 BOHANNON RD. Fairburn,  GA  30213
Product CodeHQX  
CFR Regulation Number886.3340 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-10-10
Decision Date1987-02-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.