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Profyle

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
PROFYLE FDA UDI
Generic Name
Implantable bone washer FDA UDI
Device Name
WASHERS FOR 1.7MM SCREWS FDA UDI
Model / Reference
59-17049 FDA UDI
Description
WASHERS FOR 1.7MM SCREWS FDA UDI

Identifiers

Catalog Number
59-17049 FDA UDI
Primary DI / UDI-DI
37613153159736 FDA UDI
510(k) Number
K980364 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Implantable bone washer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Implantable bone washer

Profyle 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

K980364 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 c6bdb7d4-b57a-4855-aa94-348e6fc28357 36 fields · synced May 29, 2026