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FDA 510(k)

ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202

K-Number: K870329 · 1987-02-13

Decision Date1987-02-13
Product CodeHTR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 is the device name listed in this FDA 510(k) record. The listed applicant is Biodynamic Technologies, Inc.. It received FDA 510(k) clearance on 1987-02-13 under 510(k) number K870329. The device is classified under product code HTR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202?

ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Biodynamic Technologies, Inc.. The 510(k) number is K870329.

When did ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 receive FDA 510(k) clearance?

ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870329.

Who is the listed applicant for ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202?

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

What is the FDA product code for ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202?

The FDA product code for ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #1202 is HTR.

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 Biodynamic Technologies, 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.

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Related Devices (Code: HTR)

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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