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FastForward

FDA UDI

Class II (US FDA UDI)

by Fastforward Surgical Inc

Identity

Trade Name
FastForward FDA UDI
Generic Name
Orthopaedic bone washer, sterile FDA UDI
Device Name
Plate, FastForward, Small FDA UDI
Model / Reference
1700-00-002 FDA UDI
Description
Plate, FastForward, Small FDA UDI

Identifiers

Primary DI / UDI-DI
00860003755525 FDA UDI
510(k) Number
K141420 FDA UDI
FDA Product Code
HTN FDA UDI
GMDN Term
Orthopaedic bone washer, sterile 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

No

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
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic bone washer, sterile

FastForward by Fastforward Surgical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone washer, sterile.

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 d3faf405-065c-4078-af58-741bd68add65 34 fields · synced May 30, 2026