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Vectre

FDA UDI

Class U (US FDA UDI)

by Quandary Medical Llc

Identity

Trade Name
Vectre FDA UDI
Generic Name
Bone-screw internal spinal fixation system, sterile FDA UDI
Device Name
5.0 mm x 30 mm Vectre Facet Screw, Lag FDA UDI
Model / Reference
TR1-2837 FDA UDI
Description
5.0 mm x 30 mm Vectre Facet Screw, Lag FDA UDI

Identifiers

Primary DI / UDI-DI
00815361020655 FDA UDI
510(k) Number
K073515 FDA UDI
FDA Product Code
MRW FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, sterile FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone-screw internal spinal fixation system, sterile

Vectre by Quandary Medical Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, sterile.

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 b9dba8b3-d359-40c2-a302-3f4c9009724a 34 fields · synced May 30, 2026