← Back to catalogue

FastFrame™

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
FastFrame™ FDA UDI
Generic Name
External orthopaedic fixation system, single-use, sterile FDA UDI
Model / Reference
47-5300-070-00 FDA UDI

Identifiers

Catalog Number
47-5300-070-00 FDA UDI
Primary DI / UDI-DI
00889024464087 FDA UDI
510(k) Number
K152755 FDA UDI
FDA Product Code
JDW FDA UDI
KTT FDA UDI
GMDN Term
External orthopaedic fixation system, single-use, sterile 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

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 Conditional FDA UDI

Category: External orthopaedic fixation system, single-use, sterile

FastFrame™ by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External orthopaedic fixation system, single-use, sterile.

Cleared under the same submission

K152755 also covers:

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

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 16f1d6ff-0a93-406d-b1cd-db41e266b1a9 35 fields · synced Jun 8, 2026