← Back to catalogue

Rondo'

FDA UDI

Class II (US FDA UDI)

by Citieffe

Identity

Trade Name
RONDO' FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Model / Reference
Rondo' cannulated screw ø7mm L90mm FDA UDI

Identifiers

Catalog Number
VT-72090 FDA UDI
Primary DI / UDI-DI
08051739538861 FDA UDI
510(k) Number
K113388 FDA UDI
FDA Product Code
HTY FDA UDI
HTN FDA UDI
HWC FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 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: Orthopaedic bone screw, non-bioabsorbable, sterile

Rondo' by Citieffe — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

Cleared under the same submission

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
Citieffe

Sources (1)

  • FDA UDI ee3113c4-646c-433e-b662-6f4d53c985ba 36 fields · synced Jun 8, 2026