Deploy™ Expandable Interbody System

Primary DI
00815351022706
Brand
Deploy™ Expandable Interbody System
Company
Southern Spine LLC
Model
BT-1246
Device description
Nordson Graft Cannula
Published
2022-01-10
Public version status
New
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
MAXIntervertebral fusion device with bone graft, lumbar

Product Code Classifications

CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions

SubmissionSupplement
K211845000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K211845000Deploy Expandable Interbody SystemSouthern Spine, LLC2021-11-16MAX

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00815351022706PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00815351022706008153510227068153510227060815351022706

GMDN Terms

TermDefinition
Orthopaedic graft inserterA hand-held manual surgical instrument designed to push a cartilage or bone graft into a position from which the graft can be delivered into a chondral defect [e.g., during anterior cruciate ligament (ACL) reconstruction surgery]. This device is available in a variety of designs, such as a plunger made of high-grade materials [e.g., stainless steel or titanium (Ti)] used to advance the graft down its tubular-shaped holder or possibly a bone graft funnel and into place; it is also available in a variety of sizes. 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

Other Devices From This Company

Primary DIBrandModelCatalogPublished
00815351022225Deploy™ Expandable Interbody SystemD-0008282022-01-10
00815351022232Deploy™ Expandable Interbody SystemD-0009282022-01-10
00815351022249Deploy™ Expandable Interbody SystemD-0010282022-01-10
00815351022256Deploy™ Expandable Interbody SystemD-0011282022-01-10
00815351022263Deploy™ Expandable Interbody SystemD-0012282022-01-10
00815351022270Deploy™ Expandable Interbody SystemD-0013282022-01-10
00815351022287Deploy™ Expandable Interbody SystemD-0014282022-01-10
00815351022294Deploy™ Expandable Interbody SystemD-0015282022-01-10
00815351022300Deploy™ Expandable Interbody SystemD-0016282022-01-10
00815351022317Deploy™ Expandable Interbody SystemD-0017282022-01-10
00815351022324Deploy™ Expandable Interbody SystemD-0008322022-01-10
00815351022331Deploy™ Expandable Interbody SystemD-0009322022-01-10
00815351022348Deploy™ Expandable Interbody SystemD-0010322022-01-10
00815351022478Deploy™ Expandable Interbody SystemD-0815282022-01-10
00815351022485Deploy™ Expandable Interbody SystemD-0816282022-01-10
00815351022492Deploy™ Expandable Interbody SystemD-0817282022-01-10
00815351022508Deploy™ Expandable Interbody SystemD-0810322022-01-10
00815351022515Deploy™ Expandable Interbody SystemD-0811322022-01-10
00815351022522Deploy™ Expandable Interbody SystemD-0812322022-01-10
00815351022539Deploy™ Expandable Interbody SystemD-0813322022-01-10

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