← Back to catalogue

Revere

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
REVERE FDA UDI
Generic Name
Trans-facet-screw internal spinal fixation system, sterile FDA UDI
Device Name
REVERE Lamina Hook, Transverse, Small FDA UDI
Model / Reference
124.931 FDA UDI
Description
REVERE Lamina Hook, Transverse, Small FDA UDI

Identifiers

Primary DI / UDI-DI
00849044002560 FDA UDI
510(k) Number
K061202 FDA UDI
FDA Product Code
MNH FDA UDI
NKB FDA UDI
KWP FDA UDI
MNI FDA UDI
KWQ FDA UDI
GMDN Term
Trans-facet-screw internal spinal fixation system, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
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

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
Width — 5 Millimeter FDA UDI
Height — 8 Millimeter FDA UDI
Length — 8.5 Millimeter FDA UDI

Category: Trans-facet-screw internal spinal fixation system, sterile

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

Similar devices

Also classified as Trans-facet-screw internal spinal fixation system, sterile.

Cleared under the same submission

K061202 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Globus Medical, Inc.

Sources (1)

  • FDA UDI c65ac7f4-3ab9-49e1-bfb4-0a1d8295aa99 36 fields · synced May 31, 2026