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Gruve Anterior Cervical Plate System

FDA UDI

Class II (US FDA UDI)

by Life Spine, Inc.

Identity

Trade Name
Gruve Anterior Cervical Plate System FDA UDI
Generic Name
Spinal intraoperative positioning pin, single-use FDA UDI
Device Name
Fixation Pin FDA UDI
Model / Reference
150-307 FDA UDI
Description
Fixation Pin FDA UDI

Identifiers

Catalog Number
150-307 FDA UDI
Primary DI / UDI-DI
00190837065133 FDA UDI
510(k) Number
K152282 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal intraoperative positioning pin, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal intraoperative positioning pin, single-use

Gruve Anterior Cervical Plate System by Life Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal intraoperative positioning pin, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Life Spine, Inc.

Sources (1)

  • FDA UDI 56881168-24a2-43cc-ab69-807039451df3 35 fields · synced Jun 8, 2026