FDA.reportPublic FDA data

AccuPort® Cannula

Primary DI
00889024205208
Brand
AccuPort® Cannula
Company
Zimmer Knee Creations, Inc.
Model
308.082
Catalog number
308.082
Published
2016-05-18
Public version status
Update
Distribution status
Not 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
FGYCannula, Injection
FMFSyringe, Piston
MQVFiller, Bone Void, Calcium Compound

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FGYCannula, InjectionGeneral, Plastic Surgery1
FMFSyringe, PistonGeneral Hospital2
MQVFiller, Bone Void, Calcium CompoundOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K190814000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K190814000AccuFill Bone Substitute MaterialZimmer Knee Creations2019-06-10MQV

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889024205208PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024205208008890242052088890242052080889024205208

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.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length200Millimeter
Needle Gauge8Gauge

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
484-887-8902KC.Customerservice@zimmerbiomet.com

Regulatory Flags#

DUNS number
078836317
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889024205192AccuPort® Cannula 308.081308.0812016-05-18
00889024686915SCP®4643022025-07-03
00889024686922SCP®4643032025-07-03
00889024686939SCP®4645022025-07-03
00889024686946SCP®4645032025-07-03
00889024686953SCP®5141532025-07-03
00889024686960SCP®6643412025-07-03
00889024686977SCP®6645842025-07-03
00889024205253SCP402.2012015-10-23
00889024205260Subchondroplasty® Knee Kit402.2022015-10-23
00889024205277Subchondroplasty® Knee Kit402.2032015-10-23
00889024205314SCP® Knee Kit414.5022015-10-23
00889024205321SCP® Knee Kit414.5032015-10-23
00889024205338SCP® Foot & Ankle Kit514.3022015-10-23
00889024205345SCP® Foot & Ankle Kit514.3032015-10-23
00889024205352SCP® Foot & Ankle Kit514.3152015-10-23
00889024205369SCP® Foot & Ankle Kit514.5022015-10-23
00889024205376SCP® Foot & Ankle Kit514.5032015-10-23
00889024205383SCP614.5812015-10-23
00889024205390SCP614.5822015-10-23

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
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08800045105164Feel Ject(FIS-202, U-100, 0.3 cc, 29G x 12.7mm)Feel Tech Bio Co., Ltd.FMF2026-07-29
08800045105256Feel Ject(FIS-205, U-100, 0.3 cc, 31G x 8mm)Feel Tech Bio Co., Ltd.FMF2026-07-29
08800045105492Feel Ject(FIS-213, U-100, 1.0cc, 31G x 8mm)Feel Tech Bio Co., Ltd.FMF2026-07-29
08800045105614Feel Ject(FIS-217, U-100, 0.5 cc, 31G x 6mm)Feel Tech Bio Co., Ltd.FMF2026-07-29
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10816336022275NC600300-ENFNEOCHILD, LLCFMF2026-07-23
10816336022282NC602000-ENFNEOCHILD, LLCFMF2026-07-23
10816336022442NC600100-ENFNEOCHILD, LLCFMF2026-07-23
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18257200121076O-GENESISOrthofix US LLCFMF2026-07-17
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