510(k) · Cleared
ClearedOsteosorb Tack Fixation System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Noviace Corporation · JEY Plate, Bone
Cleared on Apr 1, 2004 as substantially equivalent to K022035 (Osteomedics, Inc., 2003) after a 370-day review. Its family tree reaches back 1 generation to 2003.
- Decided
- Apr 1, 2004
- Review
- 370 days
- Class
- Class II
- Product code
- JEY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K022035 (2003). No later device cites it as a predicate yet.
- Root · 1 generation backK022035 Osteomedics Resorbable Small Fixation System, OsteosorbOsteomedics, Inc. · 2003
- This deviceK030989 Osteosorb Tack Fixation SystemNoviace Corporation · 2004
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K022035 | Osteomedics Resorbable Small Fixation System, Osteosorb | Osteomedics, Inc. | 2003 | — |
| 0 (this device) | K030989 | Osteosorb Tack Fixation System | Noviace Corporation | 2004 | — |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in JEY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new JEY device
- #1 K252246 Leforte MMF Systemscore 15.6 · 16 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K022035 | Osteomedics Resorbable Small Fixation System, OsteosorbSummary page 1…Fixation System Consists of resorbable tacks and accessory instruments, which are additional components of the Osteomedics® Resorbable Small Fixation System OstcoSorb& (K022035). Resorbable tacks are available in 1.5 mm diameter and in lengths ranging from 4-8 min. The emergency tack system consists of 1.… | 2003 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Its one ancestor has no recall.
How does its category compare?
All JEY devicesJEY Plate, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JEY
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JEY
159in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JEY
1in 2020
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JEY
1,003in 2025
MAUDE reports naming product code JEY, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 9 | 115 | 0 | 29 |
| 2008 | 7 | 84 | 3 | 24 |
| 2009 | 4 | 121 | 6 | 93 |
| 2010 | 6 | 199 | 85 | 215 |
| 2011 | 5 | 75 | 0 | 241 |
| 2012 | 10 | 194 | 0 | 428 |
| 2013 | 8 | 126 | 1 | 766 |
| 2014 | 6 | 223 | 0 | 616 |
| 2015 | 7 | 160 | 0 | 767 |
| 2016 | 1 | — | 0 | 558 |
| 2017 | 5 | 190 | 0 | 568 |
| 2018 | 7 | 255 | 0 | 608 |
| 2019 | 6 | 163 | 0 | 595 |
| 2020 | 6 | 198 | 1 | 680 |
| 2021 | 4 | 299 | 0 | 451 |
| 2022 | 5 | 135 | 0 | 344 |
| 2023 | 2 | — | 0 | 495 |
| 2024 | 5 | 159 | 0 | 696 |
| 2025 | 2 | — | 0 | 1,003 |
| 2026 | 3 | 258 | 0 | — |
What is it indicated for?
The OstcoSorb® Tack Fixation System is intended for fractures of craniofacial skeleton including, but not limited to, comminuted fractures of the nasoethmoidal and infraorbital area, comminuted fractures of the frontal sinus wall, and midfacial fractures; and reconstructive procedures of the midface or craniofacial skeleton. The OsteoSorb® Tack Fixation System stabilizes bone during healing in conjunction with appropriate postoperative immobilization.…
Read the full statement (485 words)
The OstcoSorb® Tack Fixation System is intended for fractures of craniofacial skeleton including, but not limited to, comminuted fractures of the nasoethmoidal and infraorbital area, comminuted fractures of the frontal sinus wall, and midfacial fractures; and reconstructive procedures of the midface or craniofacial skeleton. The OsteoSorb® Tack Fixation System stabilizes bone during healing in conjunction with appropriate postoperative immobilization.
The OsteoSorb® Tack Fixation System stabilizes bone during healing in conjunction with appropriate postoperative immobilization. The Osteomedics® Resorbable Tack Fixation System is not intended for use in and is contraindicated for: 1) Significant comminuted fractures or area with active infection, 2) Patient conditions including: blood supply limitation, insufficient quantity or quality of bone, or latent infections and where patient co-operation can not be guaranteed (e.g. alcoholism). 3) Mandibular tumor resection. 4) Intermaxillary fixation without an appropriate external fixation by other means. 5) This device is not designed for use in the mandible or for use in full load bearing procedures.6) when time to healing is anticipated to be greater than six weeks, and when patient has a history of adverse reaction to resorbable materials (e.g. resorbable sutures).
The OsteoSorb® Smooth Pin Fixation System intended for use in the presence of appropriate immobilization for the internal fixation of fractured non-load bearing bones, osteotomies and arthrodeses, for example in fixation of apical fragments, osteochondral fragments and cancellous/non-load bearing fragments. Correction of hallux valgus and repair of metacarpal and phalageal fusion and fracture.
The OsteoSorb® Pin Fixation System stabilizes bone during healing in conjunction with appropriate postoperative immobilization. Use is contraindicated in case where conservative (closed) treatment is appropriate, where pressure osteosynthesis is desired, where fragments are subjected to tension stress, when time to healing is anticipated to be greater than six weeks, when patient has a history of adverse reaction to resorbable materials (e.g. resorbable sutures), when use of the device without appropriate postoperative immobilization, when fractures and osteotomies is in weight bearing bone, where internal fixation is otherwise contraindicated, e.g., insufficient quantity or quality of bone and where patient co-operation cannot be guaranteed (e.g. alcoholism) where significant comminuted fractures or area with active infection. Federal (USA) laws restrict this device to sale or on the order of a physician.
The Noviace HeatingPen is used for plate bending and cutting plate, screw tip and pin. The HeatingPen device enables to mold in-situ OsteoSorb Plates to varying skeleton morphologies. The HeatingPen is a single-use, cordless and battery operated. Three (3) tips are provided - a cautery tip which is used to cut plates, screw tips and pins, a long malleable plate tip, and a short fixed plate tip, both of which will bend plates in-situ.
The Noviace HeatingBath is used to shape intra-operatively the OsteoSorb® Plate and Mesh. The Noviace™ HeatingBath is consisting of heating unit and auxiliary pan, which are fabricated from PolarWare 304 Stainless Steel. The heating unit sold non-sterilized but the auxiliary pan is sold sterilized.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K030989 · printed Nov 6, 2026
Cite this page
510(k) Report. “K030989: Osteosorb Tack Fixation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K030989
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026