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

PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)

K Number: K970418 · Decision Apr 29, 1997
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
57
Applicant Total
20
Review Days
84

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Basic Information

Device Name
PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)
K Number
K970418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1330
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pmt Corp.
Date Received
February 4, 1997
Decision Date
April 29, 1997
Product Code
GZL
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
GZL Electrode, Depth

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Other Clearances by Pmt Corp.

K Number Device Name
K122376 PMT TRUSCAN SURFACE ELECTRODE
K090733 PMT HALO SYSTEM
K082474 PMT SUBDURAL CORTICAL ELECTRODES
K042901 ENDOMARK STERILE INDIA INK
K033730 PMT SPHENOIDAL ELECTRODE AND ACCESSORY, MODEL 2101-31 AND 2102-31 SERIES
K972597 PMT NEW BEGINNINGS GELSHAPES & AMEND
K964224 STAINLESS STEEL CORTAC CORTICAL ELECTRODE(2111)/PLANTINUM CORTAC CORTICAL ELECTRODE
K935560 PMT EXTERNAL EXTERNAL DRAINAGE SYSTEM (EDS)
K933079 ELECTROCAUTERY SYSTEM MODEL 1980
K935499 PMT SILICONE SHEETING
Search all 20 clearances from Pmt Corp. →