FDA.report

C-Fuse® Cervical Intervertebral Body Fusion System

Primary DI
00815351021815
Brand
C-Fuse® Cervical Intervertebral Body Fusion System
Company
Southern Spine LLC
Model
TY-0700
Device description
Cervical Cage Tray
Published
2016-07-20
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Contact Domains

Product Codes

CodeName
ODPIntervertebral fusion device with bone graft, cervical

Product Code Classifications

CodeDeviceSpecialtyClass
ODPIntervertebral Fusion Device With Bone Graft, CervicalOrthopedic2

Premarket Submissions

SubmissionSupplement
K130948000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K130948000C-FUSE CERVICAL INTERVERTEBRAL BODY FUSION SYSTEMSouthern Spine, LLC2013-08-14ODP

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00815351021815PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00815351021815008153510218158153510218150815351021815

GMDN Terms

TermDefinition
Instrument trayA container intended to provide a suitable platform for containing many medical/surgical instruments and related items during a clinical procedure; it might in addition be used during reprocessing/sterilization procedures, however it is not dedicated to reprocessing/sterilization. It is typically designed as a shallow vessel with a raised rim, or as a deeper cassette-like device, and it might include a lid. It is designed to fit into other devices such as supply trolleys, storage systems and sterilizers. This is a reusable device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(478)330-6205donna@t3med.com

Regulatory Flags

DUNS number
794672225
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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