MEDPOR ATTRACTOR IMPLANT— 510(k) K071335

Substantially Equivalent

Porex Surgical, Inc.

FDA 510(k) clearance K071335 for MEDPOR ATTRACTOR IMPLANT, Substantially Equivalent on 2007-08-08. Applicant: Porex Surgical, Inc.. Device class: 2.

Clearance details

Applicant: Porex Surgical, Inc.
Product code: Code HPZ
Device class: Class 2
Regulation: 21 CFR 886.3320
Advisory panel: Ophthalmic
Date received: 2007-05-11
Decision date: 2007-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newnan, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HPZ

K212741 — EZYPOR2022-06-24
K123764 — DURETTE OCULAR IMPLANT2013-01-31
K110554 — BIOCERAMIC ORBITAL IMPLANT, ORBTEX2011-11-02
K112176 — SILICONE SPHERES2011-09-15
K083342 — ORBITAL RECONSTRUCTIVE IMPLANT II2009-03-12

More clearances from Porex Surgical, Inc.

K102184 — MEDPOR CONTAIN CAN IMPLANT2011-01-07
K101835 — MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 800792010-12-03
K091807 — MEDPOR FIXATION SYSTEM2010-06-28
K091120 — MEDPOR CONTAIN IMPLANT2010-03-19
K083621 — MEDPOR CUSTOMIZED SURGICAL IMPLANT2009-02-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.