The following data is part of a premarket notification filed by Porex Medical with the FDA for Porex(tm) Extra-ocular Orbital Implant.
Device ID | K863946 |
510k Number | K863946 |
Device Name: | POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT |
Classification | Implant, Orbital, Extra-ocular |
Applicant | POREX MEDICAL 500 BOHANNON RD. Fairburn, GA 30213 |
Contact | Howard A Mercer,phd |
Correspondent | Howard A Mercer,phd POREX MEDICAL 500 BOHANNON RD. Fairburn, GA 30213 |
Product Code | HQX |
CFR Regulation Number | 886.3340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-10-10 |
Decision Date | 1987-02-27 |