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FDA 510(k)

DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET

K-Number: K850255 · 1985-05-01

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1985-05-01
Product Code
DecisionSubstantially Equivalent

Device Summary

DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. It received FDA 510(k) clearance on 1985-05-01 under 510(k) number K850255. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET?

DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K850255.

When did DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET receive FDA 510(k) clearance?

DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET received FDA 510(k) clearance on 1985-05-01, under 510(k) number K850255.

Who is the listed applicant for DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMET?

The FDA 510(k) record lists Dow Corning Corp. Healthcare Industries Materials as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Dow Corning Corp. Healthcare Industries Materials 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.

K853186SILASTIC INFLATABLE BONE PLUG H.P.K844637WHITESIDE ACRYLIC CEMENT SPACER SLEEVEK843995TF-II HIP PROSTHESISK842559WHITESIDE ORTHOLOC TOTAL HIP FEMORALK840357SSA HIP PROSTHESISK831479METAL-BACKED ACETABULAR CUP

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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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