FDA.reportPublic FDA data

Sagittae

Primary DI
00819837020026
Brand
Sagittae
Company
SPINEEX, INC.
Model
010-030-46
Catalog number
010-030-46
Device description
Lateral Lumbar Interbody Fusion Device46.0 mm length x 21.5 mm width x 8.4 mm-17.1 mm height, 0°-30° lordosis
Published
2019-02-06
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
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
K181531000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K181531000SpineEX Sagittae Lateral Lumbar Interbody Fusion DevicesSpineex, Inc.2018-10-05MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00819837020026PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00819837020026008198370200268198370200260819837020026

GMDN Terms#

Term, Definition table
TermDefinition
Metallic spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Angle30degree
Height17.1Millimeter
Length46Millimeter
Width21.5Millimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
5105736165info@spineexinc.com

Regulatory Flags#

DUNS number
080723590
Device count
1
DM exempt
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00819837020019Sagittae010-030-42010-030-422019-02-06
00819837020033Sagittae010-030-50010-030-502019-02-06
00819837020040Sagittae010-030-54010-030-542019-02-06
00819837020057Sagittae010-030-58010-030-582019-02-06
00819837020309Sagittae012-030-10012-030-102020-05-14
00819837020361Sagittae012-030-20012-030-202020-05-14
00819837021108Sagittae012-030-11012-030-112020-05-14
00819837021122Sagittae012-030-21012-030-212020-05-14
00819837020071Sagittae012-030-00012-030-002019-02-06
00819837020132Sagittae521-030-00521-030-002019-02-06
00819837021207Sagittae014-030-22014-030-222020-05-14
00819837021245Sagittae075-030-10075-030-102020-05-14
00819837020064Sagittae075-030-00075-030-002019-02-06
00819837021146Sagittae076-030-00076-030-002019-10-21
00819837021283Sagittae902-030-05902-030-052021-09-22
00819837021320Sagittae902-030-15902-030-152021-09-22
00819837020804Sagittae025-030-09025-030-092020-05-14
00819837020828Sagittae025-030-10025-030-102020-05-14
00819837020842Sagittae025-030-11025-030-112020-05-14
00819837020866Sagittae025-030-12025-030-122020-05-14

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00197157076061ZAVATION DISTRACTORZavation LLCMAX2026-05-28
00197157075859ZAVATION INSERTERZavation LLCMAX2026-05-27
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B707129410010200DUALXS T/PLIF 18 DEG x 10-13MMAMPLIFY SURGICAL, INC.MAX2026-05-27
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