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Distal Tibial A-Plate

FDA UDI

Class II (US FDA UDI)

by Flower Orthopedics Corporation

Identity

Trade Name
Distal Tibial A-Plate FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
Implants for orthopedic bone fixation, compatible with 2.7mm/3.5/4.0mm screws FDA UDI
Model / Reference
DAT 005 FDA UDI
Description
Implants for orthopedic bone fixation, compatible with 2.7mm/3.5/4.0mm screws FDA UDI

Identifiers

Primary DI / UDI-DI
00840118109079 FDA UDI
510(k) Number
K133102 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Orthopaedic fixation plate, non-bioabsorbable

Distal Tibial A-Plate by Flower Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, 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 4fc11141-6df4-430d-963e-e2f75ac6cd06 35 fields · synced May 31, 2026