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

CEDAR(TM) PELVIC CUSHION

K Number: K873690 · Decision Oct 26, 1987
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
3
Applicant Total
17
Review Days
48

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Basic Information

Device Name
CEDAR(TM) PELVIC CUSHION
K Number
K873690
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cedar Surgical, Inc.
Date Received
September 8, 1987
Decision Date
October 26, 1987
Product Code
LWG
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
LWG Surgical Table Cushion

Similar 510(k) Clearances

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

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Other Clearances by Cedar Surgical, Inc.

K Number Device Name
K873692 RAYLOR(TM) DRILL STOP
K872281 RAYLOR FUSION FUNNEL
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. →