OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK— 510(k) K951811

Name: FDA 510(k) clearance K951811
Creator: U.S. Food and Drug Administration
Published: 1995-05-31

Substantially Equivalent

Osteotech, Inc.

FDA 510(k) clearance K951811 for OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK, Substantially Equivalent on 1995-05-31. Applicant: Osteotech, Inc.. Device class: 1.

Clearance details

Applicant: Osteotech, Inc.
Product code: Code LRP
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1995-04-19
Decision date: 1995-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shrewsbury, NJ, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.