Tri-Lock Long Stem Modular Neck
FDA 510(k) K864331 · Depuy, Inc.
510(k) numberK864331
Submission
- Device name
- Tri-Lock Long Stem Modular Neck
- Applicant
- Depuy, Inc.
Warsaw, IN, US - Received
- November 4, 1986
- Decision date
- January 6, 1987
- Decision
- Substantially Equivalent for Some Indications (SN)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Tri-Lock Long Stem Modular Neck cleared by the FDA?
Tri-Lock Long Stem Modular Neck (K864331) received a 510(k) decision of Substantially Equivalent for Some Indications on January 6, 1987, 63 days after the submission was received.