BRIDGE(TM) HIP SYSTEM
K-Number: K933871 · 1994-02-23
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Device Summary
Frequently Asked Questions
What is the BRIDGE(TM) HIP SYSTEM?
BRIDGE(TM) HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1994-02-23. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K933871.
When did BRIDGE(TM) HIP SYSTEM receive FDA 510(k) clearance?
BRIDGE(TM) HIP SYSTEM received FDA 510(k) clearance on 1994-02-23, under 510(k) number K933871.
Who is the listed applicant for BRIDGE(TM) HIP SYSTEM?
The FDA 510(k) record lists Wrightmedicaltechnologyinc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRIDGE(TM) HIP SYSTEM?
The FDA product code for BRIDGE(TM) HIP SYSTEM is JDG.
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 Wrightmedicaltechnologyinc 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: JDG)
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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