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FDA 510(k)

CAMLOG ABUTMENTS PS

K-Number: K090347 · 2009-06-18

ApplicantAltatec GmbH
Decision Date2009-06-18
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAMLOG ABUTMENTS PS is the device name listed in this FDA 510(k) record. The listed applicant is Altatec GmbH. It received FDA 510(k) clearance on 2009-06-18 under 510(k) number K090347. 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 CAMLOG ABUTMENTS PS?

CAMLOG ABUTMENTS PS is a medical device that received FDA 510(k) clearance on 2009-06-18. The listed applicant is Altatec GmbH. The 510(k) number is K090347.

When did CAMLOG ABUTMENTS PS receive FDA 510(k) clearance?

CAMLOG ABUTMENTS PS received FDA 510(k) clearance on 2009-06-18, under 510(k) number K090347.

Who is the listed applicant for CAMLOG ABUTMENTS PS?

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

What is the FDA product code for CAMLOG ABUTMENTS PS?

The FDA product code for CAMLOG ABUTMENTS PS is NHA.

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Other records listing Altatec GmbH 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.

K193401Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE ImplantsK160784CAM Titanium BlanksK153779Abutment for BridgesK152509CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)K113779CONELOG IMPLANT SYSTEMK103252CAMLOG VARIO SR ABUTMENTS

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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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