← Back to catalogue

Zyfix Spinal Facet Screw System

FDA UDI

Class U (US FDA UDI)

by Xtant Medical Holdings, Inc.

Identity

Trade Name
Zyfix Spinal Facet Screw System FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Zygafix COMPRESSION SCREW, 6.0 x 20MM SINGLE THREAD FDA UDI
Model / Reference
X076-0029 FDA UDI
Description
Zygafix COMPRESSION SCREW, 6.0 x 20MM SINGLE THREAD FDA UDI

Identifiers

Primary DI / UDI-DI
M697X07600291 FDA UDI
510(k) Number
K123932 FDA UDI
FDA Product Code
MRW FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
U 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

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
Length — 20 Millimeter FDA UDI
Outer Diameter — 6 Millimeter FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Zyfix Spinal Facet Screw System by Xtant Medical Holdings, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 579fc061-2c1d-439a-928f-104636844615 36 fields · synced Jun 8, 2026