Accolade

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name: Accolade FDA UDI
Generic Name: Orthopaedic cement spacer FDA UDI
Device Name: Distal Spacer FDA UDI
Model / Reference: 1059-6713 FDA UDI
Description: Distal Spacer FDA UDI

Identifiers

Catalog Number: 1059-6713 FDA UDI
Primary DI / UDI-DI: 07613327014334 FDA UDI
FDA Product Code: LZO FDA UDI
MEH FDA UDI
KWL FDA UDI
LWJ FDA UDI
MAY FDA UDI
LPH FDA UDI
MBL FDA UDI
KWY FDA UDI
JDI FDA UDI
KWZ FDA UDI
GMDN Term: Orthopaedic cement spacer FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3353 FDA UDI
888.3360 FDA UDI
888.3358 FDA UDI
888.3390 FDA UDI
888.3350 FDA UDI
888.3310 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 13.0 Millimeter FDA UDI

Category: Orthopaedic cement spacer

Accolade by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Howmedica Osteonics Corp.

Sources (1)

FDA UDI 513c218d-7a9d-4845-94cd-ebd838f64ac9 35 fields · synced May 30, 2026