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

Cadence Ankle PSI System

K Number: K241326 · Decision Aug 30, 2024
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
6
Applicant Total
12
Review Days
112

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Basic Information

Device Name
Cadence Ankle PSI System
K Number
K241326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3110
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3D Systems, Inc.
Date Received
May 10, 2024
Decision Date
August 30, 2024
Product Code
OYK
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
OYK Ankle Arthroplasty Implantation System

Similar 510(k) Clearances

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

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Other Clearances by 3D Systems, Inc.

K Number Device Name
K261826 VSP System (Titanium Palatal Splint)
K250711 VSP Orthopedics System
K243173 Salto Talaris Ankle PSI System
K243174 Cadence Ankle PSI System
K241148 Salto Talaris Ankle PSI System
K231834 VSP PEEK Cranial Implant
K231585 Vantage PSI System
K183489 D2P
K190044 VSP Orthopedics System
K161841 D2P
Search all 12 clearances from 3D Systems, Inc. →