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FDA 510(k)

SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)

K-Number: K800898 · 1980-05-02

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1980-05-02
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SILASTIC BONE PLUG H.P.(CEMENT RESTRICT) 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 1980-05-02 under 510(k) number K800898. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)?

SILASTIC BONE PLUG H.P.(CEMENT RESTRICT) is a medical device that received FDA 510(k) clearance on 1980-05-02. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K800898.

When did SILASTIC BONE PLUG H.P.(CEMENT RESTRICT) receive FDA 510(k) clearance?

SILASTIC BONE PLUG H.P.(CEMENT RESTRICT) received FDA 510(k) clearance on 1980-05-02, under 510(k) number K800898.

Who is the listed applicant for SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)?

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 SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)?

The FDA product code for SILASTIC BONE PLUG H.P.(CEMENT RESTRICT) is JDS.

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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 SLEEVEK850255DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMETK843995TF-II HIP PROSTHESISK842559WHITESIDE ORTHOLOC TOTAL HIP FEMORALK840357SSA HIP PROSTHESIS

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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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