← Back to catalogue

Prct2

FDA UDI

Class II (US FDA UDI)

by Fx Solutions

Identity

Trade Name
PRCT2 FDA UDI
Generic Name
Total shoulder prosthesis FDA UDI
Device Name
PRCT2, PRCT II HUMERAL PLATE TA6V RIGHT 4 HOLES FDA UDI
Model / Reference
100-0004 FDA UDI
Description
PRCT2, PRCT II HUMERAL PLATE TA6V RIGHT 4 HOLES FDA UDI

Identifiers

Catalog Number
100-0004 FDA UDI
Primary DI / UDI-DI
03701037301760 FDA UDI
510(k) Number
K143721 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Total shoulder prosthesis 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 80.5 Millimeter FDA UDI

Category: Total shoulder prosthesis

Prct2 by Fx Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total shoulder prosthesis.

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
Fx Solutions

Sources (1)

  • FDA UDI fa3c26aa-39c6-4195-a1e6-c1c6b5de4a3b 37 fields · synced May 30, 2026