FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

Erisma LP Navigated Instruments

K Number: K202956 · Decision Feb 26, 2021
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
11
Review Days
149

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Basic Information

Device Name
Erisma LP Navigated Instruments
K Number
K202956
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clariance, Sas
Date Received
September 30, 2020
Decision Date
February 26, 2021
Product Code
OLO
Advisory Committee
Neurology
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
OLO Orthopedic Stereotaxic Instrument

Similar 510(k) Clearances

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

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Other Clearances by Clariance, Sas

K Number Device Name
K202032 Idys LLIF 3DTi
K200920 Idys ALIF ZP 3DTi
K192168 Idys ALIF ZP 3DTi
K191263 Idys ALIF TiVac
K183259 Idys™ TLIF TiVac
K172465 Idys™ TLIF 3DTi Cages
K172083 Idys™ ALIF System
K170163 Erisma® LP Spinal Fixation System
K162367 Erisma® LP MIS
K153326 Erisma-LP Spinal Fixation System
Search all 11 clearances from Clariance, Sas →