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FDA 510(k)

HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM

K-Number: K920768 · 1992-04-21

ApplicantThe Straumann Co.
Decision Date1992-04-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM is the device name listed in this FDA 510(k) record. The listed applicant is The Straumann Co.. It received FDA 510(k) clearance on 1992-04-21 under 510(k) number K920768. 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 HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM?

HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is The Straumann Co.. The 510(k) number is K920768.

When did HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM receive FDA 510(k) clearance?

HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM received FDA 510(k) clearance on 1992-04-21, under 510(k) number K920768.

Who is the listed applicant for HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM?

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

What is the FDA product code for HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM?

The FDA product code for HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM is DZE.

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Other records listing The Straumann Co. as applicant

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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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