The following data is part of a premarket notification filed by Novabone Products, Llc with the FDA for Novabone-resorbable Bone Graft Substitute.
Device ID | K021336 |
510k Number | K021336 |
Device Name: | NOVABONE-RESORBABLE BONE GRAFT SUBSTITUTE |
Classification | Filler, Bone Void, Calcium Compound |
Applicant | NovaBone Products, LLC ONE PROGRESS BLVD. SUITE 33 Alachua, FL 32615 |
Contact | David M Gaisser |
Correspondent | David M Gaisser NovaBone Products, LLC ONE PROGRESS BLVD. SUITE 33 Alachua, FL 32615 |
Product Code | MQV |
CFR Regulation Number | 888.3045 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-04-26 |
Decision Date | 2002-07-25 |
Summary: | summary |