Atlas FDA

THE MAGNUM CHIN IMPLANT

FDA 510(k) clearance K961071 · decided 1996-04-19

Clearance details

K-number
K961071
Device name
THE MAGNUM CHIN IMPLANT
Applicant
Rand Scientific Corp.
Decision
Substantially Equivalent
Date received
1996-03-18
Decision date
1996-04-19
Days to decision
32 days
Clearance type
Traditional
Product code
FWP
Device class
2
Regulation number
878.3550
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Sacramento, CA, US
Third-party review
No
Expedited review
No

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STRYKER CMF MEDPOR CUSTOMIZED IMPLANT (K121315)Howmedica Osteonics Corp.2012-11-01
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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
TRANSAIRE(TM) RIGID GAS PERMEABLE CONTACT LENSES (P890044/S027)Rand Scientific Corp.1994-01-26
TRANSAIRE(TM) RIGID GAS PERMEABLE CONTACT LENSES (P890044/S026)Rand Scientific Corp.1993-05-27
TRANSAIRE(TM) RIGID GAS PERMEABLE CONTACT LENSES (P890044/S025)Rand Scientific Corp.1993-02-09
ADD RGP LENS FINISHING LABORATORIES. (P890044/S024)Rand Scientific Corp.1993-02-05
ADD RGP LENS FINISHING LABORATORIES. (P890044/S023)Rand Scientific Corp.1992-09-30
ADD RGP LENS FINISHING LABORATORIES. (P890044/S022)Rand Scientific Corp.1992-09-01
ADD RGP LENS FINISHING LABORATORIES. (P890044/S021)Rand Scientific Corp.1992-06-26
ADD RGP LENS FINISHING LABORATORIES. (P890044/S020)Rand Scientific Corp.1992-04-14