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

K2M MODULAR HOOKS

K Number: K133402 · Decision Jul 30, 2014
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
100
Review Days
266

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Basic Information

Device Name
K2M MODULAR HOOKS
K Number
K133402
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
K2m, Inc.
Date Received
November 6, 2013
Decision Date
July 30, 2014
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

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Other Clearances by K2m, Inc.

K Number Device Name
K260546 Q Pedicle Instruments
K253545 Vulcan Spinal System
K252873 Q Interbody Instruments
K211320 CAPRI Corpectomy Cage System
K202528 Cannulated Power Driver Attachment
K201006 K2M Navigation Instruments
K193203 MOJAVE Expandable Interbody System
K193129 Yukon OCT Spinal System
K192911 Brainlab Compatible K2M Navigation Instruments
K190179 SAHARA Stabilization System
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