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FDA PMA

Filler, bone void, synthetic peptide

PMA Number: P140019 · 2026-09-16

ApplicantCerapedics, LLC
Decision Date2026-09-16
PMA NumberP140019
Product CodeNOX
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Filler, bone void, synthetic peptide is the device name listed in this FDA 510(k) record. The listed applicant is Cerapedics, LLC. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code NOX. It was reviewed by the OR advisory panel.

Frequently Asked Questions

What is the Filler, bone void, synthetic peptide?

Filler, bone void, synthetic peptide is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Cerapedics, LLC.

When did Filler, bone void, synthetic peptide receive FDA 510(k) clearance?

The clearance date for Filler, bone void, synthetic peptide can be found in the official FDA records.

Who is the listed applicant for Filler, bone void, synthetic peptide?

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

What is the FDA product code for Filler, bone void, synthetic peptide?

The FDA product code for Filler, bone void, synthetic peptide is NOX.

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.

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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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