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

SKELETAL DYNAMICS STERILIZATION TRAYS

K Number: K102103 · Decision Dec 7, 2010
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
18
Review Days
133

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Basic Information

Device Name
SKELETAL DYNAMICS STERILIZATION TRAYS
K Number
K102103
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Skeletal Dynamics, LLC
Date Received
July 27, 2010
Decision Date
December 7, 2010
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 Skeletal Dynamics, LLC

K Number Device Name
K182492 Geminus Volar Distal Radius Plate System
K180744 Stablyx CMC Arthroplasty Implant System
K172688 Align Radial Head System
K171590 Distal Elbow Plating System
K153208 Internal Joint Stabilizer - Elbow
K150675 Dorsal Spanning Plate
K143624 Headless Compression Screw System
K140892 DISTAL ELBOW PLATING SYSTEM
K140372 FRAGMENT PLATE SYSTEM
K122310 GEMINUS FOSSA SPECIFIC PLATE SYSTEM
Search all 18 clearances from Skeletal Dynamics, LLC →