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

Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device

K Number: K173535 · Decision Feb 13, 2018
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
14
Review Days
90

Basic Information

Device Name
Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device
K Number
K173535
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Titan Spine, LLC
Date Received
November 15, 2017
Decision Date
February 13, 2018
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ODP), ordered by most recent decision date.

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Other Clearances by Titan Spine, LLC

K Number Device Name
K170399 Endoskeleton TO Interbody Fusion Device (IBD)
K163269 Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device
K153122 Endoskeleton(r) TCS System
K151596 Endoskeleton TCS Interbody Fusion Device
K142940 Endoskeleton TCS System
K141953 ENDOSKELETON; TA IBD AND VBR, TO AND TT, TAS, TC, TL
K142589 Endoskeleton TA IBD and VBR, Endoskeleton TO and TT, Endoskeleton TAS, Endoskeleton TAS, Endoskeleton TC, Endoskeleton TL
K140055 ENDOSKELETON(R) TL INTERBODY FUSION DEVICE
K111626 ENDOSKELETON(R) TAS
K102067 ENDOSKELETON TO
Search all 14 clearances from Titan Spine, LLC →