AccuPort Multi Directional Delivery Canula 8 Ga x 200 mm Drill Length

FDA UDI

Class II (US FDA UDI)

by Zimmer Knee Creations, Inc.

Identity

Trade Name: AccuPort Multi Directional Delivery Canula 8 Ga x 200 mm Drill Length FDA UDI
Generic Name: Bone grafting cannula FDA UDI
Model / Reference: 308.083 FDA UDI

Identifiers

Catalog Number: 308.083 FDA UDI
Primary DI / UDI-DI: 00889024205215 FDA UDI
510(k) Number: K190814 FDA UDI
FDA Product Code: FMF FDA UDI
MQV FDA UDI
GMDN Term: Bone grafting cannula FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5860 FDA UDI
888.3045 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 8 Gauge FDA UDI
Length — 200 Millimeter FDA UDI

Category: Bone grafting cannula

AccuPort Multi Directional Delivery Canula 8 Ga x 200 mm Drill Length by Zimmer Knee Creations, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Bone grafting cannula.

Arthrex® — Arthrex, Inc. · Class I
Bongold Bone Graft Material — Beijing Allgens Medical Science & Technology Co., Ltd. · Class II
Arthrex® — Arthrex, Inc. · Class I
Vital™ — BIOMET SPINE LLC · Class I
One-Shot — Shanghai Kinetic Medical Co., Ltd. · Class I
Vital™ — BIOMET SPINE LLC · Class I
Precision Cannula — Zimmer, Inc. · Class I
Bongold Bone Graft Material — Beijing Allgens Medical Science & Technology Co., Ltd. · Class II

Cleared under the same submission

K190814 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Zimmer Knee Creations, Inc.

Sources (1)

FDA UDI fbb62013-b951-450c-823f-6c8099439385 36 fields · synced Jun 9, 2026