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Asnis

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
ASNIS FDA UDI
Generic Name
Implantable bone washer FDA UDI
Device Name
Washer FDA UDI
Model / Reference
619990S FDA UDI
Description
Washer FDA UDI

Identifiers

Catalog Number
619990S FDA UDI
Primary DI / UDI-DI
07613327522167 FDA UDI
510(k) Number
K220319 FDA UDI
FDA Product Code
HWC FDA UDI
OUR FDA UDI
HTN FDA UDI
GMDN Term
Implantable bone washer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

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: Implantable bone washer

Asnis by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable bone washer.

Cleared under the same submission

K220319 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI d409e1f7-157f-4f2c-aca2-971ea755f1e7 36 fields · synced Jun 8, 2026