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Fuse Pedicle Screw System

FDA UDI

Class II (US FDA UDI)

by CPM Medical Consultants, LLC

Identity

Trade Name
Fuse Pedicle Screw System FDA UDI
Generic Name
Bone awl, reusable FDA UDI
Device Name
Bone Awl FDA UDI
Model / Reference
Rev A FDA UDI
Description
Bone Awl FDA UDI

Identifiers

Catalog Number
FZ-I-039 FDA UDI
Primary DI / UDI-DI
B565FZI0390 FDA UDI
510(k) Number
K182283 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone awl, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone awl, reusable

Fuse Pedicle Screw System by CPM Medical Consultants, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone awl, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 54daa3c9-e17e-4d76-a98c-df09e4f020e5 36 fields · synced May 30, 2026