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

Straumann Surgical Cassettes

K Number: K203753 · Decision Jul 29, 2021
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
24
Review Days
218

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Basic Information

Device Name
Straumann Surgical Cassettes
K Number
K203753
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Straumann USA, LLC
Date Received
December 23, 2020
Decision Date
July 29, 2021
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 Straumann USA, LLC

K Number Device Name
K241575 Straumann® Anatomic Healing Abutments XC (AHA)
K202942 Straumann 4 mm Short Implants
K192401 Straumann Screw-Retained Abutments
K190662 MRI Compatibility for Existing Straumann Dental Implant Systems
K171784 Straumann Dental Implant System
K162890 BLT 02.9mm SC, SLA or SLActive, RXD, Loxim, SC Closure Cap and Healing Abutments, SC Temporary Abutments, SC Variobase Abutments, SC CARES Abutment
K151590 Straumann RN Gold Abutment for Bridge
K150899 Straumann CARES Titanium Alloy (TAN) Abutment
K151324 Straumann Variobase for CEREC
K151247 NC Straumann Screw Retained Abutments
Search all 24 clearances from Straumann USA, LLC →