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FDA 510(k)

SOFTLINE SPRING CLIP

K-Number: K000098 · 2000-04-12

Decision Date2000-04-12
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SOFTLINE SPRING CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Novare Surgical Systems, Inc.. It received FDA 510(k) clearance on 2000-04-12 under 510(k) number K000098. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOFTLINE SPRING CLIP?

SOFTLINE SPRING CLIP is a medical device that received FDA 510(k) clearance on 2000-04-12. The listed applicant is Novare Surgical Systems, Inc.. The 510(k) number is K000098.

When did SOFTLINE SPRING CLIP receive FDA 510(k) clearance?

SOFTLINE SPRING CLIP received FDA 510(k) clearance on 2000-04-12, under 510(k) number K000098.

Who is the listed applicant for SOFTLINE SPRING CLIP?

The FDA 510(k) record lists Novare Surgical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOFTLINE SPRING CLIP?

The FDA product code for SOFTLINE SPRING CLIP is DXC.

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 Novare Surgical Systems, 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.

View all 9 devices →

Related Devices (Code: DXC)

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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