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C2 Hip

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
C2 Hip FDA UDI
Generic Name
Orthopaedic implant impactor, reusable FDA UDI
Device Name
Spherical Stem Impactor FDA UDI
Model / Reference
9045.10.251 FDA UDI
Description
Spherical Stem Impactor FDA UDI

Identifiers

Catalog Number
9045.10.251 FDA UDI
Primary DI / UDI-DI
08033390095488 FDA UDI
510(k) Number
K170473 FDA UDI
FDA Product Code
LWJ FDA UDI
KWY FDA UDI
LZO FDA UDI
GMDN Term
Orthopaedic implant impactor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
888.3390 FDA UDI
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant impactor, reusable

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

Similar devices

Also classified as Orthopaedic implant impactor, reusable.

Cleared under the same submission

K170473 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 088c2086-41d5-45b3-9703-454111198e88 35 fields · synced May 30, 2026