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Allthread Titanium

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
ALLTHREAD TITANIUM FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Model / Reference
902598 FDA UDI

Identifiers

Catalog Number
902598 FDA UDI
Primary DI / UDI-DI
00880304453463 FDA UDI
510(k) Number
K042460 FDA UDI
K080088 FDA UDI
FDA Product Code
HWC FDA UDI
GAS FDA UDI
JDR FDA UDI
MBI FDA UDI
GAT FDA UDI
MAI FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
878.5000 FDA UDI
888.3030 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

Category: Tendon/ligament bone anchor, non-bioabsorbable

Allthread Titanium by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

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 c7e0ed6b-6a33-4507-9890-2c222bd58f66 36 fields · synced May 30, 2026