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FDA 510(k)

OSTEO SMALL AND MINI BONE SCREWS

K-Number: K971778 · 1997-06-27

Decision Date1997-06-27
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEO SMALL AND MINI BONE SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Osteonics Corp.. It received FDA 510(k) clearance on 1997-06-27 under 510(k) number K971778. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEO SMALL AND MINI BONE SCREWS?

OSTEO SMALL AND MINI BONE SCREWS is a medical device that received FDA 510(k) clearance on 1997-06-27. The listed applicant is Osteonics Corp.. The 510(k) number is K971778.

When did OSTEO SMALL AND MINI BONE SCREWS receive FDA 510(k) clearance?

OSTEO SMALL AND MINI BONE SCREWS received FDA 510(k) clearance on 1997-06-27, under 510(k) number K971778.

Who is the listed applicant for OSTEO SMALL AND MINI BONE SCREWS?

The FDA 510(k) record lists Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSTEO SMALL AND MINI BONE SCREWS?

The FDA product code for OSTEO SMALL AND MINI BONE SCREWS 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 Osteonics 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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