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nexis®

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref SC060070

by Novastep

Identity

Trade Name
nexis® EUDAMEDFDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Sterile osteosynthesis screws EUDAMED
Screw Ø5 length 70 FDA UDI
Model / Reference
SC060070 EUDAMEDFDA UDI
Description
Screw Ø5 length 70 FDA UDI

Identifiers

Catalog Number
SC060070 FDA UDI
Primary DI / UDI-DI
03700879506678 EUDAMEDFDA UDI
Basic UDI-DI
370087950TF2B01020007E EUDAMED
510(k) Number
K223468 FDA UDI
FDA Product Code
HWC FDA UDI
EMDN Code
P09120601 CORTICAL SCREWS EUDAMED
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic bone screw (non-sliding)

nexis® by Novastep — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Novastep

Sources (2)

  • FDA UDI 7ce7234d-d986-47be-a8ff-c9fb2772e971 36 fields · synced Sep 17, 2026
  • EUDAMED c880a8e6-1ca1-40cd-9e59-4008399e5f64 61 fields · synced Sep 17, 2026