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Natural Nail®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Natural Nail® FDA UDI
Generic Name
Bone nail end-cap FDA UDI
Model / Reference
47-2487-001-05 FDA UDI

Identifiers

Catalog Number
47-2487-001-05 FDA UDI
Primary DI / UDI-DI
00889024094611 FDA UDI
510(k) Number
K083497 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone nail end-cap 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

No

FDA UDI

Dimensions & Sizes

Size
Height — 5 Millimeter FDA UDI

Category: Bone nail end-cap

Natural Nail® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone nail end-cap.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI b24b9e03-83b7-43ec-9e13-cf824f702b81 36 fields · synced May 30, 2026