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FDA 510(k)

ACETABULAR SCREW RING

K-Number: K833881 · 1984-01-13

ApplicantMecron Medical Products, Inc.
Decision Date1984-01-13
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACETABULAR SCREW RING is the device name listed in this FDA 510(k) record. The listed applicant is Mecron Medical Products, Inc.. It received FDA 510(k) clearance on 1984-01-13 under 510(k) number K833881. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETABULAR SCREW RING?

ACETABULAR SCREW RING is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Mecron Medical Products, Inc.. The 510(k) number is K833881.

When did ACETABULAR SCREW RING receive FDA 510(k) clearance?

ACETABULAR SCREW RING received FDA 510(k) clearance on 1984-01-13, under 510(k) number K833881.

Who is the listed applicant for ACETABULAR SCREW RING?

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

What is the FDA product code for ACETABULAR SCREW RING?

The FDA product code for ACETABULAR SCREW RING is JDI.

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Other records listing Mecron Medical Products, Inc. as applicant

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Related Devices (Code: JDI)

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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