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

Supplemental Instrument Trays

K Number: K170939 · Decision Aug 8, 2017
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
4
Review Days
131

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Basic Information

Device Name
Supplemental Instrument Trays
K Number
K170939
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuvasive Specialized Orthopedics, Incorporated
Date Received
March 30, 2017
Decision Date
August 8, 2017
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Similar 510(k) Clearances

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

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Other Clearances by Nuvasive Specialized Orthopedics, Incorporated

K Number Device Name
K233593 MAGEC Spinal Bracing and Distraction System
K232267 Precice Max System
K171791 MAGEC® System