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FDA 510(k)

FIELD ABUTMENT WEDGE

K-Number: K943343 · 1994-12-23

ApplicantMedtec, Inc.
Decision Date1994-12-23
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FIELD ABUTMENT WEDGE is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1994-12-23 under 510(k) number K943343. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIELD ABUTMENT WEDGE?

FIELD ABUTMENT WEDGE is a medical device that received FDA 510(k) clearance on 1994-12-23. The listed applicant is Medtec, Inc.. The 510(k) number is K943343.

When did FIELD ABUTMENT WEDGE receive FDA 510(k) clearance?

FIELD ABUTMENT WEDGE received FDA 510(k) clearance on 1994-12-23, under 510(k) number K943343.

Who is the listed applicant for FIELD ABUTMENT WEDGE?

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

What is the FDA product code for FIELD ABUTMENT WEDGE?

The FDA product code for FIELD ABUTMENT WEDGE is IXI.

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Other records listing Medtec, Inc. as applicant

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Related Devices (Code: IXI)

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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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