510(k) K233203
- Device
- Soft Tissue Augmentation Resorbable Matrix
- Applicant
- Collagen Matrix, Inc.
- 510(k) number
- K233203
- Product code
- NPL
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2024-05-01
- Date received
- 2023-09-28
- Regulation
- 872.3930
- Classification name
- Barrier, Animal Source, Intraoral
- Medical specialty
- Dental
- Review panel
- Dental
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- Daniel Fernandez
- Address
- 15 Thornton Rd. Oakland NJ US 07436 07436
FDA Registration Numbers
- 3013820501
- 3010155661
- 1647098
- 3002808271
- 3009443653
- 8043792
- 3008729892
- 3016668451
- 3027448274
- 3007113424
- 3004884150
- 2022435
- 1066741
- 2087119
- 2246552
- 1650372
- 3007321028
- 3013037032
- 3002808022
- 3011649314
- 3016823837
- 1313525
- 9614442
- 3009506228
- 3006017180
- 3007679154
- 3004681519
- 3003300673
- 3009039068
- 3017399129
- 2028523
- 3002924436
- 3006223010
- 3008910197
- 3004431266
- 1000393132
- 3011824442
- 1047843
- 3014448321
- 3017847628
- 2249852
- 2032542
- 3002807112
- 1319660
- 3043657402
- 2530154
- 9613348
- 3014015147
- 2245304
- 3011276344
- 1835959
- 3009598981
- 3002719998
- 3019834892
- 3014206569
- 3010097171
Source Documents
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