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Clutch

FDA UDI

Class II (US FDA UDI)

by Spinal Elements, Inc.

Identity

Trade Name
CLUTCH FDA UDI
Generic Name
Interspinous spinal fixation implant FDA UDI
Device Name
18 X 44MM FLARED Z PLATE PC FDA UDI
Model / Reference
86002-018 FDA UDI
Description
18 X 44MM FLARED Z PLATE PC FDA UDI

Identifiers

Primary DI / UDI-DI
00840606116794 FDA UDI
FDA Product Code
PEK FDA UDI
GMDN Term
Interspinous spinal fixation implant 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Interspinous spinal fixation implant

Clutch by Spinal Elements, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Interspinous spinal fixation implant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a215ac4-2a48-4047-b985-4d282e07c1c5 34 fields · synced Jun 8, 2026