ABSOLUTE ABSORBABLE INTERFERENCE SCREW
K-Number: K993975 · 1999-12-20
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Device Summary
Frequently Asked Questions
What is the ABSOLUTE ABSORBABLE INTERFERENCE SCREW?
ABSOLUTE ABSORBABLE INTERFERENCE SCREW is a medical device that received FDA 510(k) clearance on 1999-12-20. The listed applicant is Innovasive Devices, Inc.. The 510(k) number is K993975.
When did ABSOLUTE ABSORBABLE INTERFERENCE SCREW receive FDA 510(k) clearance?
ABSOLUTE ABSORBABLE INTERFERENCE SCREW received FDA 510(k) clearance on 1999-12-20, under 510(k) number K993975.
Who is the listed applicant for ABSOLUTE ABSORBABLE INTERFERENCE SCREW?
The FDA 510(k) record lists Innovasive Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABSOLUTE ABSORBABLE INTERFERENCE SCREW?
The FDA product code for ABSOLUTE ABSORBABLE INTERFERENCE SCREW is HWC. This falls under the Cardiovascular category.
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 Innovasive Devices, 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: HWC)
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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