FDA.reportPublic FDA data

Deploy™ Expandable Interbody System

Primary DI
00815351022713
Brand
Deploy™ Expandable Interbody System
Company
Southern Spine LLC
Model
RA-1341
Device description
Straight Rasp
Published
2022-01-10
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MAXIntervertebral fusion device with bone graft, lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K211845000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K211845000Deploy Expandable Interbody SystemSouthern Spine, LLC2021-11-16MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00815351022713PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00815351022713008153510227138153510227130815351022713

GMDN Terms#

Term, Definition table
TermDefinition
Bone file/rasp, manualA hand-held manual surgical instrument with a surface(s) of coarse and/or fine grooves or teeth designed to scrape and smooth the surface of bone during a surgical procedure. The device is typically a one-piece instrument with grooves/teeth along all or part of its working end(s). It is available in a variety of sizes and working end designs, including straight and curved ends and often double-ended with a central handle. It is not dedicated for use at a specific anatomy (e.g., sinus, ear) and it is made of metal [e.g., stainless steel, titanium (Ti)]. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(478)330-6205donna@t3med.com

Regulatory Flags#

DUNS number
794672225
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00815351022683Deploy™ Expandable Interbody SystemDT-12442022-01-10
00815351020009Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System10212015-10-16
00815351020016Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System10242015-10-16
00815351020023Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System10272015-10-16
00815351020030Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System10302015-10-16
00815351020047Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System10332015-10-16
00815351020054Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System20362015-10-16
00815351020061Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System20392015-10-16
00815351020078Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System20422015-10-16
00815351020085Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System20452015-10-16
00815351020092Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System20482015-10-16
00815351020108Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System30542015-10-16
00815351020115Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System30582015-10-16
00815351020122Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System30622015-10-16
00815351020139Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System30662015-10-16
00815351020146Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System30702015-10-16
00815351020153Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System40722015-10-16
00815351020160Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System40762015-10-16
00815351020177Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System40802015-10-16
00815351020184Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System40842015-10-16

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00840606185110LUNA TiSPINAL ELEMENTS, INC.MAX2026-09-25
00840606185127LUNA TiSPINAL ELEMENTS, INC.MAX2026-09-25
00840606185134LUNA TiSPINAL ELEMENTS, INC.MAX2026-09-25
00840606185141LUNA TiSPINAL ELEMENTS, INC.MAX2026-09-25
00840606185158LUNA TiSPINAL ELEMENTS, INC.MAX2026-09-25
00840606185165LUNA TiSPINAL ELEMENTS, INC.MAX2026-09-25
00840606196024VertuSPINAL ELEMENTS, INC.MAX2026-09-25
00840606196031VertuSPINAL ELEMENTS, INC.MAX2026-09-25
00840606196048VertuSPINAL ELEMENTS, INC.MAX2026-09-25
00810017915170SABER-XA, Screw Ø5.5 x 32.5ELEVATION SPINE, INC.MAX2026-09-22
10888857461819CASCADIA™ Interbody SystemVB Spine LLCMAX2019-10-31
10888857461888CASCADIA™ Interbody SystemVB Spine LLCMAX2019-10-31
04546540665720AVS NAVIGATORStryker CorporationMAX2016-09-24
10888857218772CASCADIA™ Interbody SystemVB Spine LLCMAX2015-12-16
10888857218963CASCADIA™ Interbody SystemVB Spine LLCMAX2015-12-16
10888857219076CASCADIA™ Interbody SystemVB Spine LLCMAX2015-12-16
10888857219489CASCADIA™ Interbody SystemVB Spine LLCMAX2015-12-16
10888857219595CASCADIA™ Interbody SystemVB Spine LLCMAX2015-12-16
07613153046196AVS PLStryker CorporationMAX2015-09-14
07613153046202AVS PLStryker CorporationMAX2015-09-14
07613153046219AVS PLStryker CorporationMAX2015-09-14
07613153046226AVS PLStryker CorporationMAX2015-09-14
07613153046233AVS PLStryker CorporationMAX2015-09-14
07613153046288AVS PLStryker CorporationMAX2015-09-14
07613153046295AVS PLStryker CorporationMAX2015-09-14
07613153046301AVS PLStryker CorporationMAX2015-09-14
07613153046318AVS PLStryker CorporationMAX2015-09-14
07613153046325AVS PLStryker CorporationMAX2015-09-14
07613153046332AVS PLStryker CorporationMAX2015-09-14
07613153046349AVS PLStryker CorporationMAX2015-09-14