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

PMT SUBARACHNOID SCREW, MODEL NO.1350-2

K Number: K883115 · Decision Aug 29, 1988
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
104
Applicant Total
20
Review Days
35

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Basic Information

Device Name
PMT SUBARACHNOID SCREW, MODEL NO.1350-2
K Number
K883115
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1620
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Pmt Corp.
Date Received
July 25, 1988
Decision Date
August 29, 1988
Product Code
GWM
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
GWM Device, Monitoring, Intracranial Pressure

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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
K970418 PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)
K964224 STAINLESS STEEL CORTAC CORTICAL ELECTRODE(2111)/PLANTINUM CORTAC CORTICAL ELECTRODE
K935560 PMT EXTERNAL EXTERNAL DRAINAGE SYSTEM (EDS)
K933079 ELECTROCAUTERY SYSTEM MODEL 1980
Search all 20 clearances from Pmt Corp. →