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Navigation Instrument

FDA UDI

Class II (US FDA UDI)

by Camber Spine Technologies

Identity

Trade Name
Navigation Instrument FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
5.5 mm Tap, NEO Solid, Navigation FDA UDI
Model / Reference
NAV-NEO-5500 FDA UDI
Description
5.5 mm Tap, NEO Solid, Navigation FDA UDI

Identifiers

Primary DI / UDI-DI
B030NAVNEO5500 FDA UDI
510(k) Number
K220038 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Bone tap, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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: Bone tap, reusable

Navigation Instrument by Camber Spine Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2257c6be-3924-4730-a66b-236dbffc1b51 35 fields · synced Jun 6, 2026