← Back to catalogue

Mako

FDA UDI

Class II (US FDA UDI)

by MAKO Surgical Corp.

Identity

Trade Name
Mako FDA UDI
Generic Name
Unicondylar knee prosthesis FDA UDI
Device Name
MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 10 MM FDA UDI
Model / Reference
180737-3-E FDA UDI
Description
MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 10 MM FDA UDI

Identifiers

Catalog Number
180737-3-E FDA UDI
Primary DI / UDI-DI
07613327386196 FDA UDI
FDA Product Code
HSX FDA UDI
GMDN Term
Unicondylar knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3520 FDA UDI
Commercial Distribution
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

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

Category: Unicondylar knee prosthesis

Mako by MAKO Surgical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Unicondylar knee prosthesis.

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
MAKO Surgical Corp.

Sources (1)

  • FDA UDI c5c675af-f17f-4099-8a85-f1a7dcfee3d7 35 fields · synced Jun 9, 2026