← Back to catalogue

Lcp

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
LCP FDA UDI
Generic Name
Orthopaedic bone pin, non-bioabsorbable FDA UDI
Device Name
1.8MM LCP BUTTRESS PIN 26MM FDA UDI
Model / Reference
200.197 FDA UDI
Description
1.8MM LCP BUTTRESS PIN 26MM FDA UDI

Identifiers

Catalog Number
200197 FDA UDI
Primary DI / UDI-DI
10886982141231 FDA UDI
510(k) Number
K012114 FDA UDI
K063049 FDA UDI
K091644 FDA UDI
FDA Product Code
HWC FDA UDI
HRS FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone pin, non-bioabsorbable

Lcp by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin, non-bioabsorbable.

Cleared under the same submission

K012114 also covers:

K063049 also covers:

K091644 also covers:

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
Synthes

Sources (1)

  • FDA UDI 03bee5fc-d681-4b84-9a3c-7e3d28489293 36 fields · synced May 31, 2026