510(k) K213512

Device
DERMABOND PRINEO Skin Closure System
Applicant
ETHICON, Inc.
510(k) number
K213512
Product code
OMD
Decision
Substantially Equivalent (SESE)
Decision date
2021-12-07
Date received
2021-11-02
Regulation
878.4011
Classification name
Cutaneous Tissue Adhesive With Mesh
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Noorhidayah Norizan
Address
1000 Rte. 202 S. Raritan NJ US 08869 08869

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code OMD

510(k)DeviceApplicantDecision date
K233460CM00622 LINC Skin Closure System (CM00622 LINC)Connexicon Medical , Ltd.2024-07-15
K211878LiquiBand XLAdvanced Medical Solutions Limited2022-05-23
K191461Exofin Fusion Skin Closure SystemChemence Medical, Inc.2020-06-05
K171442Exofin Fusion Skin Closure SystemChemence Medical, Inc.2017-09-25
K163645DERMABOND PRINEO Skin Closure SystemEthicon, LLC2017-04-21
K152490DERMABOND PRINEO Skin Closure SystemETHICON, Inc.2015-11-25
K133864DERMABOND PRINEO SKIN CLOSURE SYSTEMETHICON, Inc.2014-03-10
DEN090005PRINEO SKIN CLOSURE SYSTEMClosure Medical Corp.2010-04-30