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FDA 510(k)

TRI-LOCK LONG STEM MODULAR NECK

K-Number: K864331 · 1987-01-06

ApplicantDepuy, Inc.
Decision Date1987-01-06
Product Code
DecisionSubstantially Equivalent for Some Indications

Device Summary

TRI-LOCK LONG STEM MODULAR NECK is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1987-01-06 under 510(k) number K864331. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the TRI-LOCK LONG STEM MODULAR NECK?

TRI-LOCK LONG STEM MODULAR NECK is a medical device that received FDA 510(k) clearance on 1987-01-06. The listed applicant is Depuy, Inc.. The 510(k) number is K864331.

When did TRI-LOCK LONG STEM MODULAR NECK receive FDA 510(k) clearance?

TRI-LOCK LONG STEM MODULAR NECK received FDA 510(k) clearance on 1987-01-06, under 510(k) number K864331.

Who is the listed applicant for TRI-LOCK LONG STEM MODULAR NECK?

The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Depuy, Inc. 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.

K043058PINNACLE CONSTRAINED ACETABULAR LINERSK042664LPS UPPER EXTREMITYK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDER

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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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