FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STAXXSD SYSTEM

K Number: K111469 · Decision Jul 19, 2011
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
59
Review Days
53

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Basic Information

Device Name
STAXXSD SYSTEM
K Number
K111469
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Wave, Inc.
Date Received
May 27, 2011
Decision Date
July 19, 2011
Product Code
MQP
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MQP Spinal Vertebral Body Replacement Device

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Other Clearances by Spine Wave, Inc.

K Number Device Name
K260286 Dynamo™ Spinal Cement; Salvo® Spine System
K261159 Exceed® Biplanar Expandable Interbody System
K243816 Testa TP Pivoting Spacer System
K251131 Annex® 2 Adjacent Level System
K243514 Salvo® Robotic Navigation Instruments
K240685 Salvo® Spine System
K231275 Exceed™ Biplanar Expandable Interbody System
K222362 Salvo® Spine System
K202476 Salvo® Spine System
K192526 Spine Wave Navigated Instruments
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