FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

InterSpace Knee Extra-Large Size, InterSpace Knee ATS

K Number: K181732 · Decision Apr 27, 2019
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
14
Review Days
299

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Basic Information

Device Name
InterSpace Knee Extra-Large Size, InterSpace Knee ATS
K Number
K181732
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tecres S.P.A.
Date Received
July 2, 2018
Decision Date
April 27, 2019
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

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Other Clearances by Tecres S.P.A.

K Number Device Name
K252326 InterSpace GV Hip Spacer
K211163 Bone Cement Genta, Bone Cement HV, Bone Cement LV
K220131 KYPHON VuE Bone Cement
K122175 MENDEC SPINE HV, MENDEC SPINE HV SYSTEM
K112983 SPACER-S
K101356 Spacer-G and Spacer-K
K092773 CEMEX GENTA, GENTA SYSTEM AND GENTA SYSTEM FAST
K062274 SPACER-K TEMPORARY KNEE SPACER WITH GENTAMICIN, MODELS SPK0021, SPK0121, SPK0221, SPK0321
K062273 SPACER-G TEMPORARY HIP PROSTHESIS
K063438 VSPSPN
Search all 14 clearances from Tecres S.P.A. →