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FDA 510(k)

WHITESIDE ACRYLIC CEMENT SPACER SLEEVE

K-Number: K844637 · 1985-06-19

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1985-06-19
Product CodeLTC
DecisionSubstantially Equivalent

Device Summary

WHITESIDE ACRYLIC CEMENT SPACER SLEEVE 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 1985-06-19 under 510(k) number K844637. The device is classified under product code LTC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITESIDE ACRYLIC CEMENT SPACER SLEEVE?

WHITESIDE ACRYLIC CEMENT SPACER SLEEVE is a medical device that received FDA 510(k) clearance on 1985-06-19. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K844637.

When did WHITESIDE ACRYLIC CEMENT SPACER SLEEVE receive FDA 510(k) clearance?

WHITESIDE ACRYLIC CEMENT SPACER SLEEVE received FDA 510(k) clearance on 1985-06-19, under 510(k) number K844637.

Who is the listed applicant for WHITESIDE ACRYLIC CEMENT SPACER SLEEVE?

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

What is the FDA product code for WHITESIDE ACRYLIC CEMENT SPACER SLEEVE?

The FDA product code for WHITESIDE ACRYLIC CEMENT SPACER SLEEVE is LTC.

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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.K850255DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMETK843995TF-II HIP PROSTHESISK842559WHITESIDE ORTHOLOC TOTAL HIP FEMORALK840357SSA HIP PROSTHESISK831479METAL-BACKED ACETABULAR CUP

View all 31 devices →

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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