← Back to catalogue

Tarsa Link Bunion

FDA UDI

Class II (US FDA UDI)

by Life Spine, Inc.

Identity

Trade Name
Tarsa Link Bunion FDA UDI
Generic Name
Polymeric osteotomy fusion cage, non-customized FDA UDI
Device Name
Variable Angle Screw, 2.3mm x 16mm FDA UDI
Model / Reference
154-5-016 FDA UDI
Description
Variable Angle Screw, 2.3mm x 16mm FDA UDI

Identifiers

Catalog Number
154-5-016 FDA UDI
Primary DI / UDI-DI
00190837022556 FDA UDI
510(k) Number
K161037 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Polymeric osteotomy fusion cage, non-customized 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric osteotomy fusion cage, non-customized

Tarsa Link Bunion by Life Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric osteotomy fusion cage, non-customized.

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
Life Spine, Inc.

Sources (1)

  • FDA UDI b619f2dd-0216-42e4-a4f5-f57987b31e43 35 fields · synced May 30, 2026