Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NORIAN SRS FAST SET PUTTY

K-Number: K041842 · 2004-07-23

ApplicantSynthes (Usa)
Decision Date2004-07-23
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NORIAN SRS 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 2004-07-23 under 510(k) number K041842. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORIAN SRS FAST SET PUTTY?

NORIAN SRS FAST SET PUTTY is a medical device that received FDA 510(k) clearance on 2004-07-23. The listed applicant is Synthes (Usa). The 510(k) number is K041842.

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

NORIAN SRS FAST SET PUTTY received FDA 510(k) clearance on 2004-07-23, under 510(k) number K041842.

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

The FDA product code for NORIAN SRS FAST SET PUTTY is MQV.

Related Clinical Trials

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.

Other records listing Synthes (Usa) 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.

View all 409 devices →

Related Devices (Code: MQV)

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.

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.

↑