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Zavation

FDA UDI

Class II (US FDA UDI)

by Zavation

Identity

Trade Name
Zavation FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
CIF Rasp, 6 Deg, 7 & 8mm FDA UDI
Model / Reference
20-2007-02 FDA UDI
Description
CIF Rasp, 6 Deg, 7 & 8mm FDA UDI

Identifiers

Primary DI / UDI-DI
00842166195790 FDA UDI
510(k) Number
K112533 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable 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

No

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

Category: Spinal bone screw, non-bioabsorbable

Zavation by Zavation — Class II — 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

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Manufacturer

Manufacturer
Zavation

Sources (1)

  • FDA UDI 6b7eafe9-ad6e-4a9b-92ec-e563e0c646b3 35 fields · synced May 30, 2026