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Suprapatellar Tibial Entry Sheath

FDA UDI

Class II (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name
SUPRAPATELLAR TIBIAL ENTRY SHEATH FDA UDI
Generic Name
Orthopaedic implantation sleeve, single-use FDA UDI
Model / Reference
0642-000 FDA UDI

Identifiers

Primary DI / UDI-DI
00848665027624 FDA UDI
510(k) Number
K070444 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic implantation sleeve, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implantation sleeve, single-use

Suprapatellar Tibial Entry Sheath by Advanced Orthopaedic Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantation sleeve, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3105d0a-b85a-45d5-ac0a-08e40b4bf9b6 34 fields · synced May 30, 2026