SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY
K-Number: K102544 · 2011-01-05
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Device Summary
Frequently Asked Questions
What is the SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY?
SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY is a medical device that received FDA 510(k) clearance on 2011-01-05. The listed applicant is Smith & Nephew Inc., Endoscopy Div.. The 510(k) number is K102544.
When did SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY receive FDA 510(k) clearance?
SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY received FDA 510(k) clearance on 2011-01-05, under 510(k) number K102544.
Who is the listed applicant for SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY?
The FDA 510(k) record lists Smith & Nephew Inc., Endoscopy Div. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY?
The FDA product code for SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY is KCT.
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 Smith & Nephew Inc., Endoscopy Div. 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: KCT)
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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