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

VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001

K Number: K002990 · Decision Nov 6, 2000
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
49
Applicant Total
11
Review Days
42

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Basic Information

Device Name
VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001
K Number
K002990
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4460
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vascular Technology Incorporated
Date Received
September 25, 2000
Decision Date
November 6, 2000
Product Code
HBL
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
HBL Holder, Head, Neurosurgical (Skull Clamp)

Similar 510(k) Clearances

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Other Clearances by Vascular Technology Incorporated

K Number Device Name
K082870 VTI INTRAOPERATIVE DOPPLER SYSTEMS
K031091 VTI 20 MHZ GATED DOPPLER
K944764 VTI DISPOSABLE PRESSURE DISPLAY SET
K922738 VTI OXYGEN ANALYZER
K890058 VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM
K883960 GIPHY MONITOR
K864583 CARDIAC PERFORMANCE MONITOR
K862114 KHURI REGIONAL TISSUE PH MONITOR
K862113 NO. 100352 GALVANIC OXYGEN SENSOR
K852275 VASCULAR TECH # 100123 POLAROGRAPHIC OXGYEN SENSOR
Search all 11 clearances from Vascular Technology Incorporated →