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

CUI RHINOPLASTY IMPLANTS

K Number: K853945 · Decision Oct 18, 1985
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
41
Applicant Total
11
Review Days
24

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Basic Information

Device Name
CUI RHINOPLASTY IMPLANTS
K Number
K853945
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cox-Uphuff Intl.
Date Received
September 24, 1985
Decision Date
October 18, 1985
Product Code
FZE
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
FZE Prosthesis, Nose, Internal

Similar 510(k) Clearances

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

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Other Clearances by Cox-Uphuff Intl.

K Number Device Name
K874276 CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER
K874342 LIGATURE CARRIER/PACKER, HYDROXYLAPATITE
K873470 TEMPLATE
K865056 CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER
K871200 CUI NASAL SEPTUM BUTTON
K865033 BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER
K854339 CUI CHIN SIZER
K831566 CUI MAMMARY PROTHESIS SIZER
K813394 DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM
K802214 COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
Search all 11 clearances from Cox-Uphuff Intl. →