TITAN SEPARATING SPRING
K-Number: K930202 · 1993-05-27
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Device Summary
Frequently Asked Questions
What is the TITAN SEPARATING SPRING?
TITAN SEPARATING SPRING is a medical device that received FDA 510(k) clearance on 1993-05-27. The listed applicant is Ortho Spectrum, Inc.. The 510(k) number is K930202.
When did TITAN SEPARATING SPRING receive FDA 510(k) clearance?
TITAN SEPARATING SPRING received FDA 510(k) clearance on 1993-05-27, under 510(k) number K930202.
Who is the listed applicant for TITAN SEPARATING SPRING?
The FDA 510(k) record lists Ortho Spectrum, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TITAN SEPARATING SPRING?
The FDA product code for TITAN SEPARATING SPRING is DZC.
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 Ortho Spectrum, Inc. 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: DZC)
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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