Skip to main content.

MEDPOR® Porous Polyethylene Implants

Specialties:

Closure

Description:

MEDPOR Porous Polyethylene Implants is designed to provide surgeons with an expanding range of options for reconstruction and augmentation. MEDPOR is a biocompatible, porous material. The interconnecting, omni-directional pore structure may allow for fibrovascular in-growth and integration of the patient's tissue.

Features and benefits:

  • Proven material[1]
  • Easy to modify/trim
  • Post-Op fibrovascular in-growth and tissue integration[2]
  • Broad portfolio of implants designed from specific neurosurgical approaches
 
For more information

  1. ^Liu JK, Gotfried ON, Cole CD, Dougherty,WR, CouldwellWT, “MEDPOR Porous Polyethylene implant for Cranioplasty and Skull Base Reconstruction”Neurosurgery [April 2004]
  2. ^Yaremchuck, MJ, "Improving Aesthetic Outcomes after Alloplastic Chin Augmentation" Plast Reconstr Surg. [Oct 2003];112(5):1422-32.
Literature Number: CMF-BR-167_Rev. None_18543

Resource center

 

United States/English

A healthcare professional must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that healthcare professionals be trained in the use of any particular product before using it in a procedure/surgery.

The information presented is intended to demonstrate the breadth of Stryker product offerings. A healthcare professional must always refer to the package insert, product label and/or instructions for use before using any Stryker product. Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area.

Stryker or its affiliated entities own, use, or have applied for the following trademarks or service marks: Aero, Berchtold, BIO4, Clarity, CORE, Cranial iD, CranialMap, CranialMask, DirectInject, DuraMatrix, πdrive, ES2, Everest, Excelsior, FlowGate, Gateway, HydroSet, iSuite, iVAS, LITe, Maestro, Malis, MEDPOR, Mesa, MultiGen, Nano, Neuroform EZ, OASYS, SL-10, SDC3, Serengeti, Serrato, SILVERGlide, Sonopet, Spetzler, SpineJack, SpineMap, SpineMask, Stentriever, Streamline, Stryker, Stryker iD, Stryker NAV3i, Switchpoint Infinity, Synchro, Target, Target XL, TransForm, Trevo, Tritanium, Universal Neuro, Venom, Vitoss, VLIFT, Wingspan, Xia, XT-17, XT-27. All other trademarks are trademarks of their respective owners or holders.

The absence of a product, feature, or service name, or logo from this list does not constitute a waiver of Stryker’s trademark or other intellectual property rights concerning that name or logo.

DuraMatrix is a registered trademark of Collagen Matrix, Inc.

BIO4 is manufactured by Osiris Therapeutics, Inc.

Cookie disclaimer

Privacy policy

Terms of use

Surgeon disclaimer

©2019 Stryker 4100 East Milham Avenue Kalamazoo, MI 49001 US