← Back to catalogue

C2 Hip

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
C2 Hip FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
C2 Hip - Stem #11 H=180 mm - Taper 12/14 FDA UDI
Model / Reference
Stem FDA UDI
Description
C2 Hip - Stem #11 H=180 mm - Taper 12/14 FDA UDI

Identifiers

Catalog Number
4510.15.130 FDA UDI
Primary DI / UDI-DI
08033390005937 FDA UDI
510(k) Number
K170473 FDA UDI
FDA Product Code
LWJ FDA UDI
LZO FDA UDI
KWY FDA UDI
GMDN Term
Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
888.3353 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Press-fit femoral stem prosthesis

C2 Hip by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit femoral stem prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 34f160dd-51a6-497a-b913-79232dde8746 36 fields · synced May 30, 2026