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Zavation

FDA UDI

Class II (US FDA UDI)

by Zavation

Identity

Trade Name
ZAVATION FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
HA+ 4.5mmx85mm cannulated screw FDA UDI
Model / Reference
673-4585-1 FDA UDI
Description
HA+ 4.5mmx85mm cannulated screw FDA UDI

Identifiers

Primary DI / UDI-DI
00842166166912 FDA UDI
510(k) Number
K211113 FDA UDI
FDA Product Code
MNI FDA UDI
MNH FDA UDI
KWP FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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
Radiation Sterilization FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Zavation by Zavation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

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 645ec40f-a1fd-4e7d-9d6a-76e0da43337e 35 fields · synced May 30, 2026