Silc

SILC 4.75-5.5mm Inline 4mm Cord Clamp

Registry build 21.09.26
1manufacturer
8catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Registered in Shandong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OWI
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42

Record

Regulatory record for Silc
Listed by Globus Medical, Inc., United States
FDA product code OWI
Device type Bone Fixation Cerclage, Sublaminar
Device class Class 2
Regulation 21 CFR 888.3010
Establishment Manufacturer, Exporter
510(k) K133482
Record published 2015-11-07
Record revised 2025-07-02 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Sizes Width 6 to 12 mm; length 550 mm

Catalogue Numbers

Catalogue numbers for Silc
Catalogue number Size Status
1116.0155 Rod Slot Diameter 5.8 Millimeter In distribution
1116.0255 In distribution
1116.0006S Width 6 mm In distribution
1116.1350S In distribution
6116.3204 In distribution
1116.0165 Width 12 mm In distribution
1116.0147 Rod Slot Diameter 4.85 Millimeter In distribution
1116.1250S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Jazz System Implanet 118
Hiline Globus Medical, Inc. 22
Ligapass Medicrea International 20
Translace™ Spinal Tethering System Medtronic Sofamor Danek, Inc. 14
Nile™ Alternative Fixation System VB Spine LLC 13
Nile™ Proximal Fixation System VB Spine LLC 13
Universal Clamp ™ Zimmer Spine, Inc. 9
VersaTie Nuvasive, Inc. 8
Mariner Cap Seaspine Orthopedics Corporation 7
Jazz Lock Implanet 6
Invictus Alphatec Spine, Inc. 5
Karma Spinal Elements, Inc. 3

Showing 12 of 20. All products under Bone Fixation Cerclage, Sublaminar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K230565 2023-04-20
K172417 2017-10-26
K133482 2014-05-21

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer