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PlusDrive

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
PlusDrive FDA UDI
Generic Name
Craniofacial bone screw, non-bioabsorbable FDA UDI
Device Name
1.5MM TI CORTEX SCR SLF-TPNG WITH PLUSDRIVE(TM) RECESS 5MM FDA UDI
Model / Reference
400.035 FDA UDI
Description
1.5MM TI CORTEX SCR SLF-TPNG WITH PLUSDRIVE(TM) RECESS 5MM FDA UDI

Identifiers

Catalog Number
400035 FDA UDI
Primary DI / UDI-DI
20887587041916 FDA UDI
510(k) Number
K102656 FDA UDI
K980199 FDA UDI
FDA Product Code
JEY FDA UDI
DZL FDA UDI
GMDN Term
Craniofacial bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 FDA UDI
872.4880 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: Craniofacial bone screw, non-bioabsorbable

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

Similar devices

Also classified as Craniofacial 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

Manufacturer
Synthes

Sources (1)

  • FDA UDI c9f28c8b-d47b-49a9-97d9-a5e8e32d9bc7 36 fields · synced May 30, 2026