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FDA 510(k)

S-ROM SUPERCUP ACETABULAR CUP

K-Number: K870088 · 1988-04-22

Decision Date1988-04-22
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

S-ROM SUPERCUP ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Joint Medical Products Corp.. It received FDA 510(k) clearance on 1988-04-22 under 510(k) number K870088. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the S-ROM SUPERCUP ACETABULAR CUP?

S-ROM SUPERCUP ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1988-04-22. The listed applicant is Joint Medical Products Corp.. The 510(k) number is K870088.

When did S-ROM SUPERCUP ACETABULAR CUP receive FDA 510(k) clearance?

S-ROM SUPERCUP ACETABULAR CUP received FDA 510(k) clearance on 1988-04-22, under 510(k) number K870088.

Who is the listed applicant for S-ROM SUPERCUP ACETABULAR CUP?

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

What is the FDA product code for S-ROM SUPERCUP ACETABULAR CUP?

The FDA product code for S-ROM SUPERCUP ACETABULAR CUP is LWJ.

Related Clinical Trials

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.

Other records listing Joint Medical Products Corp. 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.

View all 33 devices →

Related Devices (Code: LWJ)

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.

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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