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PNP Femur

FDA UDI

Class II (US FDA UDI)

by Orthopediatrics Corp.

Identity

Trade Name
PNP Femur FDA UDI
Generic Name
Femur intramedullary nail FDA UDI
Device Name
9mm x 420mm Adolescent Nail, Left FDA UDI
Model / Reference
00-1503-0942-S FDA UDI
Description
9mm x 420mm Adolescent Nail, Left FDA UDI

Identifiers

Catalog Number
00-1503-0942-S FDA UDI
Primary DI / UDI-DI
00841132192498 FDA UDI
510(k) Number
K250623 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Femur intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Femur intramedullary nail

PNP Femur by Orthopediatrics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femur intramedullary nail.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b03b0660-0d0f-42a8-9c86-e0e2bc95e9e5 36 fields · synced Jun 8, 2026