FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BONE CUTTING INSTRUMENTS & ACCESSORIES

K Number: K874961 · Decision Dec 30, 1987
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
1
Applicant Total
13
Review Days
28

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Basic Information

Device Name
BONE CUTTING INSTRUMENTS & ACCESSORIES
K Number
K874961
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Solway, Inc.
Date Received
December 2, 1987
Decision Date
December 30, 1987
Product Code
GDR
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GDR Saw, Manual And Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GDR), ordered by most recent decision date.

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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
K875043 RONGEUR (NEUROSURGICAL INSTRUMENTS)
K874966 TUNING FORKS
K874950 MICROSURGICAL INSTRUMENTS
K874959 VASCULAR CLAMP
K874954 MANUAL RONGEUR
K874952 MANUAL CRANIAL DRILL, BURR, TREPHINE & ACCESSORIES
Search all 13 clearances from Solway, Inc. →