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Zavation Medical Products, LLC

FDA UDI

Class II (US FDA UDI)

by Zavation

Identity

Trade Name
Zavation Medical Products, LLC FDA UDI
Generic Name
Internal spinal fixation procedure kit, reusable FDA UDI
Device Name
Rod Persuader Short FDA UDI
Model / Reference
ZAV-1273 FDA UDI
Description
Rod Persuader Short FDA UDI

Identifiers

Primary DI / UDI-DI
00842166196926 FDA UDI
510(k) Number
K162575 FDA UDI
FDA Product Code
KWP FDA UDI
NKG FDA UDI
GMDN Term
Internal spinal fixation procedure kit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
888.3075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Internal spinal fixation procedure kit, reusable

Zavation Medical Products, LLC by Zavation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal spinal fixation procedure kit, reusable.

Cleared under the same submission

K162575 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zavation

Sources (1)

  • FDA UDI 30cda10c-3c5c-4288-8879-1cde0f209e8d 35 fields · synced May 30, 2026