Atlas FDA

DURALASTIC ANATOMICAL MALAR IMPLANTS

FDA 510(k) clearance K971479 · decided 1997-07-18

Clearance details

K-number
K971479
Device name
DURALASTIC ANATOMICAL MALAR IMPLANTS
Applicant
Allied Biomedical Corp.
Decision
Substantially Equivalent
Date received
1997-04-23
Decision date
1997-07-18
Days to decision
86 days
Clearance type
Traditional
Product code
LZK
Device class
2
Regulation number
878.3550
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Paso Robles, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Allied Biomedical Corp.

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
AART MALAR IMPLANT (K021419)Aesthetic and Reconstructive Technologies, Inc.2002-07-02
IMPLANTECH COMPOSITE FACIAL IMPLANTS (MALAR, CHIN, AND NASAL) (K002886)Implantech Associates, Inc.2000-11-24
PILLAR MALAR IMPLANT (K992240)Pillar Surgical, Inc.1999-11-22
SURGIFORM ANATOMICAL MALAR (K983756)Surgical Technology Laboratories, Inc.1998-11-20
SEARE BIOMEDICAL MALAR IMPLANTS (K982763)Seare Biomedical Corp.1998-09-30
SILIMED MALAR IMPLANT (K981835)Silimed, LLC1998-07-09
SPECTRUM DESIGNS PROFILE MALAR IMPLANT (K980139)Spectrum Designs, Inc.1998-03-03
SPECTRUM DESIGNS PROJECTION MALAR IMPLANT (K980141)Spectrum Designs, Inc.1998-03-03
SPECTRUM DESIGNS MEDIAL MALAR IMPLANT (K980140)Spectrum Designs, Inc.1998-03-03
IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT (K973502)Implantech Associates, Inc.1997-11-07
DURALASTIC ANATOMICAL MALAR IMPLANT (K973574)Hanson Medical, Inc.1997-10-24
BONE SOURCE HYDROXYAPATITE (K970400)Orthofix, Inc.1997-05-02

Recalls involving this device

No recalls on record reference this clearance.