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

Mini Sterilizable Tray

K Number: K200858 · Decision Aug 6, 2020
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
17
Review Days
127

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Basic Information

Device Name
Mini Sterilizable Tray
K Number
K200858
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implant Direct Sybron Manufacturing, LLC
Date Received
April 1, 2020
Decision Date
August 6, 2020
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

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Other Clearances by Implant Direct Sybron Manufacturing, LLC

K Number Device Name
K231087 Guided Surgery Kit
K223535 SMARTbase Abutment System
K222211 Implant Direct Dental Implant Systems Portfolio - MR Conditional
K202524 Standard Sterilizable Tray
K201553 Simply Iconic Implants
K200265 Surgical Drills
K192221 Legacy2, Legacy3, Legacy4, simplyLegacy2, simplyLegacy3 dental implants; Legacy2, Legacy3, Legacy4 fixture-mounts
K192218 Custom Legacy and Custom InterActive Titanium Abutments
K191458 Legacy SMARTBase Abutments
K181359 InterActive SMARTBase Abutments
Search all 17 clearances from Implant Direct Sybron Manufacturing, LLC →