Cannulated Screws

FDA UDI

Class II (US FDA UDI)

by aap Implantate AG

Identity

Trade Name: Cannulated Screws FDA UDI
Generic Name: Implantable bone washer FDA UDI
Device Name: Washer, I-ø2.2, O-ø4.5 Titanium FDA UDI
Model / Reference: SU 0205-00-2 FDA UDI
Description: Washer, I-ø2.2, O-ø4.5 Titanium FDA UDI

Identifiers

Catalog Number: SU 0205-00-2 FDA UDI
Primary DI / UDI-DI: 04042409088384 FDA UDI
510(k) Number: K990776 FDA UDI
FDA Product Code: HTN FDA UDI
GMDN Term: Implantable bone washer 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

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Implantable bone washer

Cannulated Screws by aap Implantate AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable bone washer.

ISOLA — Depuy Spine, Inc. · Class II
Spiked Gridlock Screw Washer — Trilliant Surgical LLC · Class II
Monster Screw System — Paragon 28 · Class II
ALPHALOK Plating System — Vilex, Inc. · Class II
Monster Screw System — Paragon 28 · Class II
FLAT WASHER — Biomet Orthopedics, Inc. · Class II
Fixcet Spinal Facet Screw System — Xtant Medical Holdings, Inc. · U
LEOS Cannulated Screw System — Tyber Medical · Class II

Cleared under the same submission

K990776 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: aap Implantate AG

Sources (1)

FDA UDI e7ab8097-17c8-4110-aceb-396c51f5123a 35 fields · synced May 30, 2026