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NOVA Minimally Invasive System

FDA UDI

Class II (US FDA UDI)

by Baui Biotech Co. Ltd.

Identity

Trade Name
NOVA Minimally Invasive System FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Nova Poly Axial Screw FDA UDI
Model / Reference
663-6535A FDA UDI
Description
Nova Poly Axial Screw FDA UDI

Identifiers

Primary DI / UDI-DI
04712899251772 FDA UDI
510(k) Number
K242899 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone screw, non-bioabsorbable

NOVA Minimally Invasive System by Baui Biotech Co. Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

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 57adeb9d-dc24-407e-bcbc-7b2d3ec12a6b 34 fields · synced Jun 1, 2026