← Back to catalogue

Cslp

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
CSLP FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
TI CERVICAL SPINE LOCKING PL VARIABLE ANGLE 1 LEVEL/26MM FDA UDI
Model / Reference
450.157 FDA UDI
Description
TI CERVICAL SPINE LOCKING PL VARIABLE ANGLE 1 LEVEL/26MM FDA UDI

Identifiers

Catalog Number
450157 FDA UDI
Primary DI / UDI-DI
10705034780832 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

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: Spinal fixation plate, non-bioabsorbable

Cslp by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI 3305377b-a8ab-4666-9f05-1e448f807dfe 35 fields · synced May 31, 2026