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Keel Lock Implant System

FDA UDI

Class I (US FDA UDI)

by Crossroads Extremity Systems Llc

Identity

Trade Name
Keel Lock Implant System FDA UDI
Generic Name
Orthopaedic chisel FDA UDI
Device Name
KEEL-LOCK BROACH ASSEMBLY FDA UDI
Model / Reference
KEEL-LOCK BROACH ASSEMBLY FDA UDI
Description
KEEL-LOCK BROACH ASSEMBLY FDA UDI

Identifiers

Catalog Number
248520PKG FDA UDI
Primary DI / UDI-DI
00810112598049 FDA UDI
FDA Product Code
HTQ FDA UDI
GMDN Term
Orthopaedic chisel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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

Yes

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: Orthopaedic chisel

Keel Lock Implant System by Crossroads Extremity Systems Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic chisel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Crossroads Extremity Systems Llc

Sources (1)

  • FDA UDI 37bdd6a8-8f37-456b-9dec-8e46ea4b72b5 34 fields · synced Jun 6, 2026