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Tspace® Peek

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
TSPACE® PEEK FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
TSPACE PEEK IMPLANT 5° 34X11.5X9MM FDA UDI
Model / Reference
SJ969P FDA UDI
Description
TSPACE PEEK IMPLANT 5° 34X11.5X9MM FDA UDI

Identifiers

Catalog Number
SJ969P FDA UDI
Primary DI / UDI-DI
04046963805906 FDA UDI
FDA Product Code
MAX 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

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

Category: Polymeric spinal interbody fusion cage

Tspace® Peek by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI ee4999f9-49b0-4e72-8b0e-e996fa9b3745 36 fields · synced May 31, 2026