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Affixus®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Affixus® FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Model / Reference
814650095 FDA UDI

Identifiers

Catalog Number
814650095 FDA UDI
Primary DI / UDI-DI
00887868139642 FDA UDI
510(k) Number
K150867 FDA UDI
K241651 FDA UDI
FDA Product Code
HSB FDA UDI
JDS FDA UDI
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
888.3030 FDA UDI
888.3040 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)

Affixus® by Zimmer, Inc. — 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

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI a53ea8c6-5c00-4659-9ca9-e85c1472849d 36 fields · synced Jun 8, 2026