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Zavation

FDA UDI

Class U (US FDA UDI)

by Zavation

Identity

Trade Name
Zavation FDA UDI
Generic Name
Lumbar interspinous decompression instrument set, reusable FDA UDI
Device Name
Large Dilator FDA UDI
Model / Reference
290-1005 FDA UDI
Description
Large Dilator FDA UDI

Identifiers

Primary DI / UDI-DI
00842166180703 FDA UDI
510(k) Number
K132126 FDA UDI
FDA Product Code
MRW FDA UDI
GMDN Term
Lumbar interspinous decompression instrument set, reusable FDA UDI

Classification

Device Class
U 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: Lumbar interspinous decompression instrument set, reusable

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

Similar devices

Also classified as Lumbar interspinous decompression instrument set, reusable.

Cleared under the same submission

K132126 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 b300a50a-66a7-4ff9-8cd6-41947d19b4ba 35 fields · synced Jun 8, 2026