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Stasys-C Standalone PEEK

FDA UDI

Class II (US FDA UDI)

by Genesys Orthopedics Systems LLC

Identity

Trade Name
Stasys-C Standalone PEEK FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
6mm AIS-C II Cervical Standalone, Small, Parallel PEEK Interbody FDA UDI
Model / Reference
1 FDA UDI
Description
6mm AIS-C II Cervical Standalone, Small, Parallel PEEK Interbody FDA UDI

Identifiers

Catalog Number
ACC800-06S FDA UDI
Primary DI / UDI-DI
M719ACC80006S0 FDA UDI
510(k) Number
K242483 FDA UDI
FDA Product Code
OVE FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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: Polymeric spinal interbody fusion cage

Stasys-C Standalone PEEK by Genesys Orthopedics Systems LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

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 3d871033-17f5-4df4-b8cb-47a85903a342 36 fields · synced May 30, 2026