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Escalade Acetabular System

FDA UDI

Class II (US FDA UDI)

by Ortho Development Corp.

Identity

Trade Name
Escalade Acetabular System FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Dia.6.5x40mm Cancellous Bone Screw Low Profile FDA UDI
Model / Reference
170-2040 FDA UDI
Description
Dia.6.5x40mm Cancellous Bone Screw Low Profile FDA UDI

Identifiers

Primary DI / UDI-DI
00822409017430 FDA UDI
510(k) Number
K103384 FDA UDI
FDA Product Code
LPH FDA UDI
LZO FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 40 Millimeter FDA UDI
Outer Diameter — 6.5 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Escalade Acetabular System by Ortho Development Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 33ded478-30bf-4f19-9522-5011da1b80a2 36 fields · synced Jun 1, 2026