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AlignMate

FDA UDI

Class II (US FDA UDI)

by Arthrosurface Incorporated

Identity

Trade Name
AlignMate FDA UDI
Generic Name
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile FDA UDI
Device Name
Bone Plate, Right 34mm FDA UDI
Model / Reference
9B00-200R-A FDA UDI
Description
Bone Plate, Right 34mm FDA UDI

Identifiers

Catalog Number
9B00-200R-A FDA UDI
Primary DI / UDI-DI
M5289B00200RA0 FDA UDI
510(k) Number
K162391 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

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

AlignMate 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

K162391 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 5b5dc3bc-f8ff-4239-8ab3-ac830a1b9a91 36 fields · synced May 30, 2026