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

FlareHawk Interbody Fusion System

K Number: K183184 · Decision Apr 3, 2019
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
11
Review Days
135

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Basic Information

Device Name
FlareHawk Interbody Fusion System
K Number
K183184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Integrity Implants, Inc.
Date Received
November 19, 2018
Decision Date
April 3, 2019
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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

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Other Clearances by Integrity Implants, Inc.

K Number Device Name
K231098 LineSider® Spinal System
K213355 Toro-L Interbody Fusion System
K220453 FlareHawk Interbody Fusion System
K212088 Integrity Implants Navigated Instruments
K203038 Toro-L Interbody Fusion System
K203367 LineSider™ Spinal System
K202198 FlareHawk Interbody Fusion System
K201367 FlareHawk TiHawk9 Interbody Fusion System
K190360 LineSider™ Spinal System
K182114 FlareHawk Interbody Fusion System
Search all 11 clearances from Integrity Implants, Inc. →