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FDA 510(k)

ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY

K-Number: K152969 · 2016-03-31

ApplicantConmed Corporation
Decision Date2016-03-31
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2016-03-31 under approval number K152969. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY?

ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY is a medical device that received FDA 510(k) clearance on 2016-03-31. It is manufactured by Conmed Corporation. The 510(k) number is K152969.

When was ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY approved by the FDA?

ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY received FDA 510(k) clearance on 2016-03-31, under approval number K152969.

What company makes ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY?

ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY is manufactured by Conmed Corporation.

What is the FDA product code for ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY?

The FDA product code for ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY is KCT.

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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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