← Back to catalogue

Spiked Gridlock Screw Washer

FDA UDI

Class II (US FDA UDI)

by Trilliant Surgical LLC

Identity

Trade Name
Spiked Gridlock Screw Washer FDA UDI
Generic Name
Implantable bone washer FDA UDI
Model / Reference
303-50-002 FDA UDI

Identifiers

Primary DI / UDI-DI
00812926023601 FDA UDI
510(k) Number
K130964 FDA UDI
FDA Product Code
NDG 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Implantable bone washer

Spiked Gridlock Screw Washer by Trilliant Surgical LLC — 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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 543232a3-0776-41d8-9723-a5afdced46ae 34 fields · synced Jun 1, 2026