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Zavation Pedicle Probe

FDA UDI

Class I (US FDA UDI)

by Zavation

Identity

Trade Name
ZAVATION PEDICLE PROBE FDA UDI
Generic Name
Stereotactic surgery system probe, reusable FDA UDI
Device Name
TIGER 2 PEDICLE PROBE, CURVED LENKE FDA UDI
Model / Reference
989-1004 FDA UDI
Description
TIGER 2 PEDICLE PROBE, CURVED LENKE FDA UDI

Identifiers

Primary DI / UDI-DI
00197157013042 FDA UDI
510(k) Number
K243908 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Stereotactic surgery system probe, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Stereotactic surgery system probe, reusable

Zavation Pedicle Probe by Zavation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stereotactic surgery system probe, reusable.

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 4c10374d-97e6-44f8-8db5-7af10f4b3eff 35 fields · synced Jun 8, 2026