CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS
K-Number: K050548 · 2005-04-01
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Device Summary
Frequently Asked Questions
What is the CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS?
CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS is a medical device that received FDA 510(k) clearance on 2005-04-01. The listed applicant is Surgical Specialties Corp. The 510(k) number is K050548.
When did CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS receive FDA 510(k) clearance?
CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS received FDA 510(k) clearance on 2005-04-01, under 510(k) number K050548.
Who is the listed applicant for CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS?
The FDA 510(k) record lists Surgical Specialties Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS?
The FDA product code for CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS is GAW.
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 Surgical Specialties Corp 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.
Related Devices (Code: GAW)
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.
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