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Canopy

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
CANOPY FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
CANOPY Shelf Plate, In-line, 9mm FDA UDI
Model / Reference
1102.3009 FDA UDI
Description
CANOPY Shelf Plate, In-line, 9mm FDA UDI

Identifiers

Primary DI / UDI-DI
00889095027679 FDA UDI
510(k) Number
K121732 FDA UDI
FDA Product Code
NQW FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 9 Millimeter FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

Canopy by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

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 e2f92ac4-50f5-4d5f-8b0a-6d63f2efec34 36 fields · synced Jun 8, 2026