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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
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
5.0mm x 44mm Partially Threaded Recon Screw FDA UDI
Model / Reference
00-1506-5044-S FDA UDI
Description
5.0mm x 44mm Partially Threaded Recon Screw FDA UDI

Identifiers

Catalog Number
00-1506-5044-S FDA UDI
Primary DI / UDI-DI
00841132195086 FDA UDI
510(k) Number
K250623 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) 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: Orthopaedic bone screw (non-sliding)

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

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

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 380d9f0d-9413-4b06-a3d1-bdd5505dc696 36 fields · synced May 31, 2026