Atlas FDA

CUI RHINOPLASTY IMPLANTS

FDA 510(k) clearance K853945 · decided 1985-10-18

Clearance details

K-number
K853945
Device name
CUI RHINOPLASTY IMPLANTS
Applicant
Cox-Uphuff Intl.
Decision
Substantially Equivalent
Date received
1985-09-24
Decision date
1985-10-18
Days to decision
24 days
Clearance type
Traditional
Product code
FZE
Device class
2
Regulation number
878.3680
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Santa Barbara, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Cox-Uphuff Intl.

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Medicon Epiplating System (K241253)Cmf Medicon Surgical, Inc.2024-12-12
Osseointegrated Fixtures (K161548)Southern Implants (Pty), Ltd.2016-12-01
HANSON MEDICAL FACIAL IMPLANTS (K090803)Hanson Medical, Inc.2010-06-30
NOBEL BIOCARE ENDOSSEOUS IMPLANTS (MAXILLOFACIAL INDICATION) (K090630)Nobel Biocare AB2009-06-02
MONARCH NASAL IMPLANT (K071018)Hanson Medical, Inc.2007-05-25
MONARCH NASAL IMPLANT (K041690)Hanson Medical, Inc.2005-02-11
AART NASAL IMPLANT (K021418)Aesthetic and Reconstructive Technologies, Inc.2002-07-02
PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS (K992242)Pillar Surgical, Inc.1999-11-22
NASAL DORSAL SERIES (K983755)Surgical Technology Laboratories, Inc.1998-11-20
SEARE BIOMEDICAL NASAL IMPLANTS (K982753)Seare Biomedical Corp.1998-09-30
SILIMED NASAL L SHAPED IMPLANT (K981833)Silimed, LLC1998-06-26
DURALASTIC ANATOMICAL NASAL IMPLANTS (K973573)Hanson Medical, Inc.1997-11-13

Recalls involving this device

No recalls on record reference this clearance.