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

RONGEUR (NEUROSURGICAL INSTRUMENTS)

K Number: K875043 · Decision Jan 22, 1988
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
35
Applicant Total
13
Review Days
51

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Basic Information

Device Name
RONGEUR (NEUROSURGICAL INSTRUMENTS)
K Number
K875043
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4840
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Solway, Inc.
Date Received
December 2, 1987
Decision Date
January 22, 1988
Product Code
HAE
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
HAE Rongeur, Manual

Similar 510(k) Clearances

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Other Clearances by Solway, Inc.

K Number Device Name
K874960 CARDIOVASCULAR SURGICAL INSTRUMENTS
K874962 FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS
K874956 SELF-RETAINING RETRACTOR FOR NEUROSURGERY
K874964 DENTAL HAND INSTRUMENTS
K874966 TUNING FORKS
K874950 MICROSURGICAL INSTRUMENTS
K874959 VASCULAR CLAMP
K874954 MANUAL RONGEUR
K874952 MANUAL CRANIAL DRILL, BURR, TREPHINE & ACCESSORIES
K874965 MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE
Search all 13 clearances from Solway, Inc. →