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

POREX QUALITY PLASTIC SURGERY INSTRUMENTS

K Number: K872947 · Decision Aug 21, 1987
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
10
Applicant Total
15
Review Days
24

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Basic Information

Device Name
POREX QUALITY PLASTIC SURGERY INSTRUMENTS
K Number
K872947
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Porex Medical
Date Received
July 28, 1987
Decision Date
August 21, 1987
Product Code
KDG
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
KDG Chisel (Osteotome)

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Other Clearances by Porex Medical

K Number Device Name
K872791 POREX NERVE LOCATOR
K873044 POREX OTOLOGY INSTRUMENTS
K863943 POREX(TM) EYE SPHERE IMPLANT
K863946 POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT
K870154 POREX(TM) TISSUE EXPANDER
K870182 POREX(TM) MALAR IMPLANT
K870257 POREX(TM) SILICONE SURGICAL IMPLANTS FOR E.N.T.
K863939 POREX(TM) EAR PROSTHESIS
K863942 POREX(TM) NOSE PROSTHESIS
K863941 POREX(TM) PROSTHESIS, CHIN, INTERNAL
Search all 15 clearances from Porex Medical →