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7.3mm BONE-LOK Implant

FDA UDI

Class II (US FDA UDI)

by Interventional Spine, Inc

Identity

Trade Name
7.3mm BONE-LOK Implant FDA UDI
Generic Name
Bone-screw internal spinal fixation system, sterile FDA UDI
Device Name
7.3mm Diameter by 90-100mm Length FDA UDI
Model / Reference
TLCD-73-90100S FDA UDI
Description
7.3mm Diameter by 90-100mm Length FDA UDI

Identifiers

Catalog Number
9015-03 FDA UDI
Primary DI / UDI-DI
81195401085024 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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
MRI Safety
MR Safe FDA UDI

Category: Bone-screw internal spinal fixation system, sterile

7.3mm BONE-LOK Implant by Interventional Spine, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Interventional Spine, Inc

Sources (1)

  • FDA UDI b7bbb313-4ce1-4635-bd0b-d27d108b94ec 35 fields · synced Jun 1, 2026