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FDA 510(k)

IMPLANT, SILICONE AND TANTALUM

K-Number: K760550 · 1976-10-05

ApplicantMedical Instrument Research Assoc., Inc.
Decision Date1976-10-05
Product CodeHQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

IMPLANT, SILICONE AND TANTALUM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instrument Research Assoc., Inc.. It received FDA 510(k) clearance on 1976-10-05 under 510(k) number K760550. The device is classified under product code HQJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANT, SILICONE AND TANTALUM?

IMPLANT, SILICONE AND TANTALUM is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Medical Instrument Research Assoc., Inc.. The 510(k) number is K760550.

When did IMPLANT, SILICONE AND TANTALUM receive FDA 510(k) clearance?

IMPLANT, SILICONE AND TANTALUM received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760550.

Who is the listed applicant for IMPLANT, SILICONE AND TANTALUM?

The FDA 510(k) record lists Medical Instrument Research Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLANT, SILICONE AND TANTALUM?

The FDA product code for IMPLANT, SILICONE AND TANTALUM is HQJ.

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Other records listing Medical Instrument Research Assoc., 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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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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