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Truliant CC

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Truliant CC FDA UDI
Generic Name
Knee arthroplasty wedge FDA UDI
Device Name
TRULIANT AUG. BLOCK SZ 5, 15MM DIST/10MM POST FDA UDI
Model / Reference
02-010-07-5510 FDA UDI
Description
TRULIANT AUG. BLOCK SZ 5, 15MM DIST/10MM POST FDA UDI

Identifiers

Catalog Number
02-010-07-5510 FDA UDI
Primary DI / UDI-DI
10885862613097 FDA UDI
510(k) Number
K150890 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Knee arthroplasty wedge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Knee arthroplasty wedge

Truliant CC by Exactech, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee arthroplasty wedge.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Exactech, Inc.

Sources (1)

  • FDA UDI a77e58e2-cc69-4312-aaac-d224de38b33a 35 fields · synced Jun 1, 2026