Sochi

FDA UDI

Class II (US FDA UDI)

by Altus Spine

Identity

Trade Name: Sochi FDA UDI
Generic Name: Spinal bone set screw FDA UDI
Device Name: Locking Screw FDA UDI
Model / Reference: A16-17-0000 FDA UDI
Description: Locking Screw FDA UDI

Identifiers

Primary DI / UDI-DI: 00843210167299 FDA UDI
510(k) Number: K210887 FDA UDI
FDA Product Code: KWP FDA UDI
NKG FDA UDI
GMDN Term: Spinal bone set screw FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3050 FDA UDI
888.3075 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone set screw

Sochi by Altus Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K210887 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Altus Spine

Sources (1)

FDA UDI 3c399a2b-b2c0-410f-a470-06bf85e700ab 35 fields · synced Jun 1, 2026