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Ankle Suture Button

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Ankle Suture Button FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
Ankle Suture Button for Use Within Plate Slot FDA UDI
Model / Reference
SYN-001-01 FDA UDI
Description
Ankle Suture Button for Use Within Plate Slot FDA UDI

Identifiers

Catalog Number
SYN-001-01 FDA UDI
Primary DI / UDI-DI
00846832056651 FDA UDI
FDA Product Code
HTN FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Ankle Suture Button by Tornier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI d9731239-8596-4fd7-8b13-3908be81c776 36 fields · synced May 30, 2026