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FDA 510(k)

IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013

K-Number: K960480 · 1996-03-15

ApplicantVident
Decision Date1996-03-15
Product CodeELL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 is the device name listed in this FDA 510(k) record. The listed applicant is Vident. It received FDA 510(k) clearance on 1996-03-15 under 510(k) number K960480. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013?

IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 is a medical device that received FDA 510(k) clearance on 1996-03-15. The listed applicant is Vident. The 510(k) number is K960480.

When did IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 receive FDA 510(k) clearance?

IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 received FDA 510(k) clearance on 1996-03-15, under 510(k) number K960480.

Who is the listed applicant for IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013?

The FDA 510(k) record lists Vident as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013?

The FDA product code for IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 is ELL.

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Other records listing Vident as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K063768TITANIUM SCALLOPED ABUTMENTK060441VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98K052710VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,K052130VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40K050362VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)K022996VITA IN-CERAM YZ CUBES FOR CEREC

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Related Devices (Code: ELL)

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K240586Additive Manufacturing Zirconia Customized RestorationHangzhou Thales Medtech Co., Ltd.K203072Franz Zirconia Dental CrownFranz Biotech, Inc.K162043NobelProcera HT ML FCZ BridgeNobel Biocare ABK153534NobelProcera HT ML Full Contour Zirconia CrownNobel Biocare ABK071182PROCERA BRIDGE ZIRCONIA 9 UNITS-14 UNITS, MODELS 30-4004 TO 30-4013Nobel Biocare ABK060530SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.Lifecore Biomedical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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