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FDA 510(k)

STRYKER PRECISION DENTAL IMPLANT SYSTEM

K-Number: K921805 · 1994-03-10

ApplicantStryker Instruments
Decision Date1994-03-10
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STRYKER PRECISION DENTAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 1994-03-10 under 510(k) number K921805. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER PRECISION DENTAL IMPLANT SYSTEM?

STRYKER PRECISION DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-10. The listed applicant is Stryker Instruments. The 510(k) number is K921805.

When did STRYKER PRECISION DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?

STRYKER PRECISION DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 1994-03-10, under 510(k) number K921805.

Who is the listed applicant for STRYKER PRECISION DENTAL IMPLANT SYSTEM?

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

What is the FDA product code for STRYKER PRECISION DENTAL IMPLANT SYSTEM?

The FDA product code for STRYKER PRECISION DENTAL IMPLANT SYSTEM is DZE.

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Related Devices (Code: DZE)

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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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