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Restoris

FDA UDI

Class II (US FDA UDI)

by MAKO Surgical Corp.

Identity

Trade Name
RESTORIS FDA UDI
Generic Name
Patellofemoral joint prosthesis FDA UDI
Device Name
MCK Patellofemoral Component FDA UDI
Model / Reference
180411 FDA UDI
Description
MCK Patellofemoral Component FDA UDI

Identifiers

Catalog Number
180411 FDA UDI
Primary DI / UDI-DI
00848486002558 FDA UDI
510(k) Number
K082172 FDA UDI
K090763 FDA UDI
K150307 FDA UDI
FDA Product Code
NPJ FDA UDI
HRY FDA UDI
HSX FDA UDI
KRR FDA UDI
GMDN Term
Patellofemoral joint prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
888.3530 FDA UDI
888.3520 FDA UDI
888.3540 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
MRI Safety
MR Conditional FDA UDI

Category: Patellofemoral joint prosthesis

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

Similar devices

Also classified as Patellofemoral joint prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MAKO Surgical Corp.

Sources (1)

  • FDA UDI b9b41cf3-a4a7-49de-b956-96d3016c5c91 36 fields · synced Jun 9, 2026