← Back to catalogue

Anterior Bone Impactor

FDA UDI

Class II (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
Anterior Bone Impactor FDA UDI
Generic Name
External spinal fixation system FDA UDI
Device Name
Anterior Bone Impactor Tip Size 9x23mm length 34cm FDA UDI
Model / Reference
7439-50 FDA UDI
Description
Anterior Bone Impactor Tip Size 9x23mm length 34cm FDA UDI

Identifiers

Catalog Number
7439-50 FDA UDI
Primary DI / UDI-DI
10840199500564 FDA UDI
510(k) Number
K875290 FDA UDI
FDA Product Code
KWP FDA UDI
GMDN Term
External spinal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: External spinal fixation system

Anterior Bone Impactor by Koros USA, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External spinal fixation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Koros USA, Inc.

Sources (1)

  • FDA UDI 4219161e-4be2-41d0-b0c4-8b577299ab25 38 fields · synced May 30, 2026