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FDA 510(k)

P.T.H. METAL-BACKED ACETABULAR CUP

K-Number: K870234 · 1987-03-20

ApplicantOrthopaedic Device Corp.
Decision Date1987-03-20
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

P.T.H. METAL-BACKED ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Orthopaedic Device Corp.. It received FDA 510(k) clearance on 1987-03-20 under 510(k) number K870234. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.T.H. METAL-BACKED ACETABULAR CUP?

P.T.H. METAL-BACKED ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Orthopaedic Device Corp.. The 510(k) number is K870234.

When did P.T.H. METAL-BACKED ACETABULAR CUP receive FDA 510(k) clearance?

P.T.H. METAL-BACKED ACETABULAR CUP received FDA 510(k) clearance on 1987-03-20, under 510(k) number K870234.

Who is the listed applicant for P.T.H. METAL-BACKED ACETABULAR CUP?

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

What is the FDA product code for P.T.H. METAL-BACKED ACETABULAR CUP?

The FDA product code for P.T.H. METAL-BACKED ACETABULAR CUP is JDL.

Related Clinical Trials

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Other records listing Orthopaedic Device 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.

K862460FEMORAL HEMI-HIP PROSTHESISK863343SUPERFIXATION(TM)K855228FEMORAL HEMI-HIP PROSTHESES

Related Devices (Code: JDL)

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.

K073499VERSYS EPOCH FULLCOAT HIP PROSTHESIS, MODEL 4088 SERIESZimmer, Inc.K070785DYNASTY ACETABULAR SYSTEMWrightmedicaltechnologyincK061844DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINERWrightmedicaltechnologyincK051995PROFEMUR RENAISSANCE HIP STEMWrightmedicaltechnologyincK051348CONSERVE TOTAL FEMORAL HEADWrightmedicaltechnologyincK042841M2A/C2A ACETABULAR SYSTEMBiomet, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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