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FDA 510(k)

MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS

K-Number: K013964 · 2002-01-24

ApplicantCp Medical
Decision Date2002-01-24
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS is the device name listed in this FDA 510(k) record. The listed applicant is Cp Medical. It received FDA 510(k) clearance on 2002-01-24 under 510(k) number K013964. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS?

MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS is a medical device that received FDA 510(k) clearance on 2002-01-24. The listed applicant is Cp Medical. The 510(k) number is K013964.

When did MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS receive FDA 510(k) clearance?

MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS received FDA 510(k) clearance on 2002-01-24, under 510(k) number K013964.

Who is the listed applicant for MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS?

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

What is the FDA product code for MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS?

The FDA product code for MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS is KXK.

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Other records listing Cp Medical 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: KXK)

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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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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