FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03

K Number: K032115 · Decision Oct 10, 2003
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
39
Applicant Total
9
Review Days
93

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Basic Information

Device Name
NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03
K Number
K032115
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5275
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Polyganics B.V.,
Date Received
July 9, 2003
Decision Date
October 10, 2003
Product Code
JXI
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JXI Cuff, Nerve

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K Number Device Name
K141816 HEMOPORE
K141423 NASOPORE-FD
K112267 NEUROLAC(R) NERVE GUIDE
K070715 NASOPORE EAR
K062540 NASOPORE EAR, MODELS ND04, ND05
K052099 NASOPORE NASAL DRESSING, MODEL NDOX-YYY/ZZ
K050573 NEUROLAC NERVE GUIDE
K042811 VIVOSORB SHEET, MODEL FS01