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FDA 510(k)

NORIAN CRS FAST SET PUTTY

K-Number: K060443 · 2006-04-13

ApplicantSynthes (Usa)
Decision Date2006-04-13
Product CodeGXP
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NORIAN CRS FAST SET PUTTY is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2006-04-13 under 510(k) number K060443. The device is classified under product code GXP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORIAN CRS FAST SET PUTTY?

NORIAN CRS FAST SET PUTTY is a medical device that received FDA 510(k) clearance on 2006-04-13. The listed applicant is Synthes (Usa). The 510(k) number is K060443.

When did NORIAN CRS FAST SET PUTTY receive FDA 510(k) clearance?

NORIAN CRS FAST SET PUTTY received FDA 510(k) clearance on 2006-04-13, under 510(k) number K060443.

Who is the listed applicant for NORIAN CRS FAST SET PUTTY?

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

What is the FDA product code for NORIAN CRS FAST SET PUTTY?

The FDA product code for NORIAN CRS FAST SET PUTTY is GXP.

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Other records listing Synthes (Usa) as applicant

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Related Devices (Code: GXP)

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.

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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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