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Meniscus Allograft Transplantation (MAT)

FDA UDI

Class I (US FDA UDI)

by Rti Surgical, Inc.

Identity

Trade Name
Meniscus Allograft Transplantation (MAT) FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Box Cutter 8mm FDA UDI
Model / Reference
999007 FDA UDI
Description
Box Cutter 8mm FDA UDI

Identifiers

Catalog Number
999007 FDA UDI
Primary DI / UDI-DI
00191083044521 FDA UDI
FDA Product Code
FZT FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

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: Orthopaedic surgical procedure kit, non-medicated, reusable

Meniscus Allograft Transplantation (MAT) by Rti Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rti Surgical, Inc.

Sources (1)

  • FDA UDI 510aeb7e-732b-4cb7-8128-d06a46fa5d64 35 fields · synced Jun 8, 2026