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

MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-2020

K Number: K021604 · Decision Jul 29, 2002
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
49
Applicant Total
19
Review Days
74

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Basic Information

Device Name
MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-2020
K Number
K021604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4460
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ohio Medical Instrument Co., Inc.
Date Received
May 16, 2002
Decision Date
July 29, 2002
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)

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Other Clearances by Ohio Medical Instrument Co., Inc.

K Number Device Name
K013428 MAYFIELD/ACCISS OPERATING ARM SYSTEM AND MAYFIELD/OPTICAL ACCISS SYSTEM
K992843 THE MAYFIELD / ACCISS SYSTEM WITH WINDOWS NT FOR CRANIAL SURGERY, THE MAYFIELD / OPTICAL ACCISS SYSTEM WITH WINDOWS NT F
K991267 SPINE APPLICATIONS FOR THE MAYFIELD/ACCISS OPERATING ARM AND OPTICAL ACCISS SYSTEMS MODULE, MAYFIELD/ACCISS SPINE RING A
K983282 OMI OCCIPITAL CERVICAL LOOP, MODEL A1089
K982244 MAYFIELD ACCISS OPTICAL SYSTEM
K960807 TEW CRANIAL/SPINAL RETRACTOR MODEL A1090
K953124 MAYFIELD RADIOLUCENT 2000 SKULL CLAMP
K941558 MAYFIELD CHILD DISPOSABLE SKULL PIN
K934289 MAYFIELD RADIOLUCENT SKULL CLAMP
K932807 MAYFIELD* A-2000 SKULL CLAMP
Search all 19 clearances from Ohio Medical Instrument Co., Inc. →