Atlas FDA

SEARE BIOMEDICAL NASAL IMPLANTS

FDA 510(k) clearance K982753 · decided 1998-09-30

Clearance details

K-number
K982753
Device name
SEARE BIOMEDICAL NASAL IMPLANTS
Applicant
Seare Biomedical Corp.
Decision
Substantially Equivalent
Date received
1998-08-06
Decision date
1998-09-30
Days to decision
55 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
Salt Lake City, UT, US
Third-party review
No
Expedited review
No

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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
SILIMED NASAL L SHAPED IMPLANT (K981833)Silimed, LLC1998-06-26
DURALASTIC ANATOMICAL NASAL IMPLANTS (K973573)Hanson Medical, Inc.1997-11-13
DURALASTIC ANATOMICAL NASAL IMPLANTS (K971481)Allied Biomedical Corp.1997-07-18

Recalls involving this device

No recalls on record reference this clearance.