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FDA 510(k)

STRAUMANN TEMPORARY COPING

K-Number: K041070 · 2004-07-23

ApplicantThe Straumann Co.
Decision Date2004-07-23
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STRAUMANN TEMPORARY COPING 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 2004-07-23 under 510(k) number K041070. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRAUMANN TEMPORARY COPING?

STRAUMANN TEMPORARY COPING is a medical device that received FDA 510(k) clearance on 2004-07-23. The listed applicant is The Straumann Co.. The 510(k) number is K041070.

When did STRAUMANN TEMPORARY COPING receive FDA 510(k) clearance?

STRAUMANN TEMPORARY COPING received FDA 510(k) clearance on 2004-07-23, under 510(k) number K041070.

Who is the listed applicant for STRAUMANN TEMPORARY COPING?

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 STRAUMANN TEMPORARY COPING?

The FDA product code for STRAUMANN TEMPORARY COPING is NHA.

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Other records listing The Straumann Co. 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.

K040646STRAUMANN GRANULESK040469THE STRAUMANN ORTHO IMPLANT SYSTEMK993862MODUS SAGITTAL SPLIT PLATEK962023PLASTIC PROTECTION HEALING CAPSK960634TITANIUM HEALING CAPSK955281ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES

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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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