FDA.reportPublic FDA data

DragonWing

Primary DI
00857373006128
Brand
DragonWing
Company
AVITUS ORTHOPAEDICS, INC.
Model
AD-5ch-5.2-120
Catalog number
AD-5ch-5.2-120
Device description
Avitus DragonWing Large Volume Autograft Delivery (Ø5.2mm, 120mm system)
Published
2023-08-28
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
FMFSyringe, Piston

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMFSyringe, PistonGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K231456000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K231456000Avitus® DragonWing Large Volume Autograft Delivery SystemAvitus Orthopaedics, Inc.2023-07-17FMF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00857373006128PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00857373006128008573730061288573730061280857373006128

GMDN Terms#

Term, Definition table
TermDefinition
Bone grafting cannulaA rigid tube intended to be used surgically to introduce a bone void filler (e.g., a bone matrix implant/bone substitute) in voids or gaps of the skeletal system (i.e., extremities, craniofacial bone, spine, and pelvis) to fill defects in the bone structure created surgically or traumatically. It is typically made of metal materials (e.g., high-grade stainless steel) with or without a plastic hub at the distal end to connect to a syringe or other device that propels the filler. The device may also be used for the delivery of orthopaedic cement. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
8606379922neil@avitusortho.com
8603727213maxim@avitusortho.com

Regulatory Flags#

DUNS number
078269403
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00857373006012Avitus Pilot Hole Creator, Disposable - 8mmPC-200PC-2002022-12-08
00857373006067Avitus Pilot Hole Creator, Disposable - 11mmPC-100PC-1002022-12-08
00857373006104Avitus Pilot Hole Creator - 11mmPH11PH112022-12-08
00857373006135Avitus Surgical TrayST-01ST-012022-12-08
00857373006142Avitus ® Bone DebriderTM – Ø8mm, 255mm Shaft LengthBH-330BH-3302024-07-08
00857373006111ArchiMISAD-1ch-4.0-120AD-1ch-4.0-1202023-07-19
00857373006074Avitus Bone HarvesterBH-220BH-2202020-10-08
00857373006005Avitus Bone HarvesterBH8BH82016-05-23
00857373006029Avitus Bone HarvesterFI-100FI-1002017-11-07
00857373006036Avitus Bone HarvesterBH-210BH-2102017-11-03
00857373006050Avitus Bone HarvesterBH-110BH-1102018-03-16

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00884450492888Merit Medical®Merit Medical Systems, Inc.FMF2026-07-22
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10383017593411Ultra-Fine SAFETYEmbecta Medical II, LLCFMF2026-07-21
10383017593510Ultra-Fine SAFETYEmbecta Medical II, LLCFMF2026-07-21
10383017593718Ultra-Fine SAFETYEmbecta Medical II, LLCFMF2026-07-21
10383017844612Ultra-Fine SAFETYEmbecta Medical II, LLCFMF2026-07-21
10383017844711Ultra-Fine SAFETYEmbecta Medical II, LLCFMF2026-07-21
10383017844919Ultra-Fine SAFETYEmbecta Medical II, LLCFMF2026-07-21
18257200121076O-GENESISOrthofix US LLCFMF2026-07-17
18257200121083O-GENESISOrthofix US LLCFMF2026-07-17
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