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PolyLock Ankle

FDA UDI

Class II (US FDA UDI)

by Fusion Orthopedics, Llc

Identity

Trade Name
PolyLock Ankle FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Hook Caddy (Aluminum) (NOT IN USE) FDA UDI
Model / Reference
TN-TR-0054-A FDA UDI
Description
Hook Caddy (Aluminum) (NOT IN USE) FDA UDI

Identifiers

Catalog Number
TN-TR-0054-A FDA UDI
Primary DI / UDI-DI
00840124513709 FDA UDI
510(k) Number
K211843 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

PolyLock Ankle by Fusion Orthopedics, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, 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 9e1c9c26-3ddf-4f2d-9646-e9cd54adf54d 35 fields · synced May 30, 2026