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Accolade

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
Accolade FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
132 Degree Neck Angle Hip Stem FDA UDI
Model / Reference
6020-2530 FDA UDI
Description
132 Degree Neck Angle Hip Stem FDA UDI

Identifiers

Catalog Number
6020-2530 FDA UDI
Primary DI / UDI-DI
04546540510617 FDA UDI
FDA Product Code
MEH FDA UDI
MBL FDA UDI
LPH FDA UDI
MAY FDA UDI
LZO FDA UDI
JDI FDA UDI
KWL FDA UDI
KWZ FDA UDI
KWY FDA UDI
LWJ FDA UDI
GMDN Term
Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3358 FDA UDI
888.3350 FDA UDI
888.3360 FDA UDI
888.3310 FDA UDI
888.3390 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Press-fit femoral stem prosthesis

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

Similar devices

Also classified as Press-fit femoral stem prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0a6990b9-a13f-4087-bf26-242444d966f7 35 fields · synced May 30, 2026