Acl Crosspin

FDA UDI

Class II (US FDA UDI)

by Biomet Sports Medicine

Identity

Trade Name: ACL CROSSPIN FDA UDI
Generic Name: Orthopaedic bone pin, bioabsorbable FDA UDI
Model / Reference: 905856 FDA UDI

Identifiers

Catalog Number: 905856 FDA UDI
Primary DI / UDI-DI: 00880304421318 FDA UDI
510(k) Number: K014305 FDA UDI
K033519 FDA UDI
FDA Product Code: MAI FDA UDI
HTY FDA UDI
JDR FDA UDI
HRS FDA UDI
GMDN Term: Orthopaedic bone pin, bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Orthopaedic bone pin, bioabsorbable

Acl Crosspin by Biomet Sports Medicine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin, bioabsorbable.

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OSSIOfiber™ Hammertoe Fixation Implant — OSSIO LTD · Class II
OSSIOfiber® Trimmable Fixation Nail System, Cannulated — OSSIO LTD · Class I
Self-Reinforced Technology — Conmed Corporation · Class II
AESCULAP — AESCULAP, INC. · Class II
SmartNail Self-Reinforced Technology — Conmed Corporation · Class II
ActivaPin™ — Bioretec Oy · Class II

Cleared under the same submission

K014305 also covers:

K033519 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Biomet Sports Medicine

Sources (1)

FDA UDI efdc2cfb-5a45-46a0-a248-f3da10ad0e9d 36 fields · synced May 29, 2026