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Summit

FDA UDI

Class II (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
SUMMIT FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Device Name
SUMMIT FEMORAL STEM 12/14 TAPER TAPERED w/DUOFIX HA SIZE 1 HI 125mm FDA UDI
Model / Reference
1570-12-070 FDA UDI
Description
SUMMIT FEMORAL STEM 12/14 TAPER TAPERED w/DUOFIX HA SIZE 1 HI 125mm FDA UDI

Identifiers

Catalog Number
157012070 FDA UDI
Primary DI / UDI-DI
10603295060123 FDA UDI
FDA Product Code
LZO FDA UDI
JDI FDA UDI
LPH FDA UDI
MEH FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3350 FDA UDI
888.3358 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Coated femoral stem prosthesis, modular

Summit by Depuy Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated femoral stem prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9c5aa288-b65b-4722-a74b-b180b545bad0 35 fields · synced Jun 8, 2026