← Back to catalogue

Easystep

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
EASYSTEP FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
Step (12mm) Staple FDA UDI
Model / Reference
EZS-12 FDA UDI
Description
Step (12mm) Staple FDA UDI

Identifiers

Catalog Number
EZS-12 FDA UDI
Primary DI / UDI-DI
07613327135237 FDA UDI
510(k) Number
K160813 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic bone staple, non-adjustable

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

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

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

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 9484e2b8-8995-4654-91fd-18a2741038f0 35 fields · synced May 30, 2026