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CheckMate®

FDA UDI

Class II (US FDA UDI)

by Arthrosurface Incorporated

Identity

Trade Name
CheckMate® FDA UDI
Generic Name
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile FDA UDI
Device Name
Pin Kit, Metatarso-Phalangeal FDA UDI
Model / Reference
9F00-1050 FDA UDI
Description
Pin Kit, Metatarso-Phalangeal FDA UDI

Identifiers

Catalog Number
9F00-1050 FDA UDI
Primary DI / UDI-DI
M5289F0010500 FDA UDI
510(k) Number
K113762 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile 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

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

Category: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

CheckMate® by Arthrosurface Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile.

Cleared under the same submission

K113762 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arthrosurface Incorporated

Sources (1)

  • FDA UDI 8dfe7e27-11cc-46a4-b309-6560d8f03550 36 fields · synced May 30, 2026