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

RAYLOR FUSION FUNNEL

K Number: K872281 · Decision Nov 2, 1987
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
3
Applicant Total
17
Review Days
139

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Basic Information

Device Name
RAYLOR FUSION FUNNEL
K Number
K872281
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cedar Surgical, Inc.
Date Received
June 16, 1987
Decision Date
November 2, 1987
Product Code
HXR
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
HXR Spatula, Orthopedic

Similar 510(k) Clearances

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Other Clearances by Cedar Surgical, Inc.

K Number Device Name
K873692 RAYLOR(TM) DRILL STOP
K873690 CEDAR(TM) PELVIC CUSHION
K873691 CEDAR(TM) RETRACTOR RING
K864425 RAYLOR(TM) DISSECTING HOOK
K864424 RAYLOR(TM) PROTECTIVE RETRACTOR
K864426 RAYLOR(TM) DEPTH GAUGE
K864421 RAYLOR(TM) PERIOSTEAL ELEVATORS
K864423 RAYLOR(TM) OSTEOTOMES
K864422 RAYLOR(TM) MALLET
K863415 RAYLOR BONE IMPACTORS
Search all 17 clearances from Cedar Surgical, Inc. →